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Production of 4-hydroxy-1,2-benzothiazine-3-carboxamides |
| RE29669 |
Production of 4-hydroxy-1,2-benzothiazine-3-carboxamides
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| Patent Drawings: | |
| Inventor: |
Lombardino |
| Date Issued: |
June 13, 1978 |
| Application: |
05/746,186 |
| Filed: |
November 30, 1976 |
| Inventors: |
Lombardino; Joseph G. (Niantic, CT)
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| Assignee: |
Pfizer, Inc. (New York, NY) |
| Primary Examiner: |
Ford; John M. |
| Assistant Examiner: |
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| Attorney Or Agent: |
Connolly and Hutz |
| U.S. Class: |
544/49; 546/309; 548/195; 548/246; 560/13; 564/194; 564/197 |
| Field Of Search: |
260/243R |
| International Class: |
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| U.S Patent Documents: |
3591584 |
| Foreign Patent Documents: |
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| Other References: |
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| Abstract: |
A process for the synthesis of N-aryl-3,4-dihydro-2-alkyl-4-oxo-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxides by treatment of N-aryl-N'-alkyl-N'-(2'-alkoxycarbonylbenzenesulfonyl)glycineamides, useful intermediates for said process, with an alkali or alkaline earth metal hydride in a reaction-inert solvent at 50.degree.-150.degree. C., said products being antiinflammatory agents. |
| Claim: |
What is claimed is:
1. A process for the preparation of a compound of the formula: ##STR10## wherein R.sub.1 is selected from the group consisting of phenyl; monosubstituted phenyl wherein saidsubstituent is selected from the group consisting of fluoro, chloro, methyl and methoxy; 2-thiazolyl; 4,5-dimethyl-2-thiazolyl; 2-pyridyl; 6-methyl-2-pyridyl, and 5-methyl-3-isoxazolyl;
R.sub.2 is alkyl containing from 1 to 3 carbon atoms; and
X is a substituent selected from the group consisting of hydrogen, methyl, methoxy, fluoro, chloro and bromo, which comprises contacting a compound of the formula: ##STR11## wherein R.sub.3 is alkyl containing from 1 to 3 carbon atoms, with ametal hydride selected from the group consisting of alkali and alkaline earth metal hydrides, in a reaction-inert solvent at 50.degree.-150.degree. C.
2. The process of claim 1 wherein the metal hydride is sodium hydride.
3. The process of claim 2 wherein the solvent is tetrahydrofuran.
4. The process of claim 3 wherein X is hydrogen, and R.sub.2 and R.sub.3 are each methyl.
5. The process of claim 4 wherein R.sub.1 is phenyl.
6. The process of claim 4 wherein R.sub.1 is 2-thiazolyl.
7. The process of claim 4 wherein R.sub.1 is 6-methyl-2-pyridyl.
8. The process of claim 4 wherein R.sub.1 is 2-pyridyl. |
| Description: |
BACKGROUND OF THE INVENTION
This invention relates to a process for the synthesis of 1,2-benzothiazine-3-carboxamides, and in particular to the preparation of N-aryl-3,4-dihydro-2-alkyl-4-oxo-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxides, a class of compounds useful asantiinflammatory agents, and to N-aryl-N'-alkyl-N'-(2'-alkoxycarbonylbenzenesulfonyl)glycineamides as useful intermediates for said process.
Synthesis of 3,4-dihydro-2-alkyl-4-oxo-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxides has been previously achieved by amination of the corresponding 3-carboxylic acid ester or by treatment of the parent3,4-dihydro-2-alkyl-4-oxo-2H-1,2-benzothiazine 1,1-dioxide with the appropriate isocyanate, Lombardino, et al., J. Med. Chem., 14, 1171 (1971) and Zinnes, et al., ibid., 16, 43 (1973) and U.S. Pat. No. 3,591,584. In addition, Zinnes, et al., loc. cit, has taught the preparation of 3-carboxamides by treatment of the pyrrolidine enamine of 3,4-dihydro-2-methyl-4-oxo-2H-1,2-benzothiazine 1,1-dioxide with phosgene followed by treatment of the resulting 3-carbonyl chloride with an appropriate amine.
U.S. Pat. No. 3,714,155 discloses 4-hydroxy-2,-N-dimethyl-2H-1,2-benzothiazine-3-carboxanilide 1,1-dioxides as antiinflammatory agents, synthesized by methylation of the corresponding N-phenyl carboxamide with dimethylsulfate in the presence ofsodium hydride.
SUMMARY OF THE INVENTION
It has now been discovered that preparation of compounds of the formula ##STR1## wherein R.sub.1 is selected from the group consisting of pheny; monosubstituted phenyl wherein said substituent is fluoro, chloro, methyl or methoxy; 2-thiazolyl;4,5-dimethyl-2-thiazolyl; 2-pyridyl; 6-methyl-2-pyridyl; and 5-methyl-3-isoxazolyl; R.sub.2 is alkyl containing one to three carbon atoms; and X is a substitutent selected from the group consisting of hydrogen, methyl, methoxy, fluoro, chloro and bromo,which comprises contacting a compound of the formula: ##STR2## wherein R.sub.3 is alkyl containing from 1 to 3 carbon atoms, with an alkali or alkaline earth metal hydride in a reaction-inert solvent at 50.degree.-150.degree. C. leads to the desiredcompounds which are potent nonsteroidal antiinflammatory agents.
Also claimed, as useful intermediates leading to the final products, are compounds of the formula ##STR3## wherein R.sub.1 is selected from the group consisting of phenyl; monosubstituted phenyl wherein said substituent is fluoro, chloro, methylor methoxy; 2-thiazolyl; 4,5-dimethyl-2-thiazolyl; 2-pyridyl; 6-methyl-2-pyridyl; and 5-methyl-3-isoxazolyl; R.sub.2 is alkyl containing one to three carbon atoms; and X is a substituent selected from the group consisting of hydrogen, methyl, methoxy,fluoro, chloro and bromo.
Also considered within the scope of the instant invention is the process wherein R.sub.3 is alkyl of up to 8 carbon atoms, aryl or aralkyl, and wherein the metal hydride is replaced by a suitable organometallic reagent.
A preferred feature of the process leading to the compounds of the present invention is the use of sodium hydride as the metal hydride and tetrahydrofuran as the reaction-inert solvent, while the preferred intermediates areN-(aryl)-N'-methyl-N'-(2'-alkoxycarbonylbenzenesulfonyl)glycineamides.
DETAILED DESCRIPTION OF THE INVENTION
The aforementioned reaction is depicted in the following scheme ##STR4## wherein R.sub.1, R.sub.2, R.sub.3 and X are as previously described.
In the above reaction of the benzenesulfonylglycineamide with a metal hydride the ratio of reactants is two equivalents of hydride per mole of glycineamide. In practice, a slight excess of 5-10 percent over two equivalents of the metal hydridehas no deleterious effect on the formation of the desired product.
It is also desirable to conduct said reaction in a reaction-inert solvent. By such a solvent, or mixtures thereof, is contemplated those, which under the conditions of the instant process, do not enter into appreciable reaction with either thestarting reagents or products. It is preferred that non-aqueous, aprotic, polar solvents be employed. Suitable solvents or mixtures thereof which are included in this group are alicyclic ethers, di(lower)-alkoxyalkanes, di(lower)alkylsulfoxides,di(lower)alkyl(lower)alkanoic amides and hexa(lower)alkylphosphoramides. Favored solvents for the present process invention are tetrahydofuran, dioxane, dimethylformamide and dimethylsulfoxide. The especially preferred solvent is tetrahydrofuran.
It is also preferred, although not a requirement, that the employed solvent be water-miscible.
Reaction time is not critical and in inherently dependent on concentration, reaction temperature and reactivity of the starting materials. In general, when temperatures of 50.degree.-100.degree. C. are employed, the reaction time will varybetween 4-10 hours.
Regarding temperature range, it is preferred, for practical reasons, that the instantly claimed process be heated in order to obtain optimum yields of the desired products. A temperature range of 50.degree.-150.degree. C. is operative, with apreferred range of 50.degree.-100.degree. C.
At the conclusion of the cyclization reaction the mixture is cooled and added to water, to which is then added sufficient acid to render the mixture acidic to litmus paper. The product is then extracted with a water-immiscible solvent, such asmethylene chloride or chloroform, and the organic extracts concentrated to dryness. Further purification of the product is effected by recrystallization from an appropriate solvent.
The intermediate benzenesulfonylglycineamides, which are cyclized under the conditions of the present process, are prepared as shown by the following flow diagram: ##STR5##
The glycine derivatives (1) are readily prepared by the methods reviewed by Greenstein and Winitz, "Chemistry of the Amino Acids," John Wiley & Sons, Inc., New York, New York 1961, Volumes 1-3.
As previously mentioned, the compounds of the present process invention are useful as antiinflammatory agents, and U.S. Pat. No. 3,591,584 teaches how to use these compounds for this utility. Of particular interest in the present invention arethe synthesis of benzothiazine 1,1-dioxide wherein R.sub.2 is methyl, X is hydrogen and R.sub.1 is phenyl, 2-pyridyl, 2-thiazolyl or 6-methyl-2-pyridyl.
The particularly preferred benzenesulfonylglycineamide intermediates are those wherein R.sub.1 is phenyl, pyridyl, 2-thiazolyl or 6-methyl-2-pyridyl and R.sub.2 and R.sub.3 are each methyl.
The examples which follow are given by way ofillustration, and are not to be construed as limitations of this invention, many variations of which are possible within the scope and spirit thereof.
EXAMPLE 1
N-(2-Thiazolyl)-3,4-dihydro-2-methyl-4-oxo-2H-1,2-benzothiazine-3-carboxami de 1,1-dioxide
To 25 mg. (0.068 m mole) of N-(2-thiazolyl)-N'-methyl-N'-(2'-methoxycarbonylbenzenesulfonyl)glycineami de in 2 ml. of dry tetrahydrofuran maintained under a nitrogen atmosphere is added 6.5 mg. (0.135 m mole) of a 50% sodium hydride suspensionin oil, and the resulting reaction mixture heated under reflux overnight. The reaction mixture comprised of a yellow suspension is quenched with ice and subsequently acidified with 2N hydrochloric acid. The product is extracted with chloroform and theextracts combined and dried over sodium sulfate. The drying agent is filtered and the filtrate concentrated to a gum, which on trituration with 0.5 ml. of chloroform and 3 ml. of hexane yields 3.3 mg. of the desired product, m.p. 172.degree.-193.degree. C. Recrystallization, m.p. 256.degree. C. dec., provides material identical to that prepared in U.S. Pat. No. 3,591,584.
EXAMPLE 2
3,4-Dihydro-2-methyl-4-oxo-2H-1,2-benzothiazinecarboxanilide 1,1-dioxide
To a solution of 3.77 g. (0.01 mole) of N-phenyl-N'-methyl-N'-(2-ethoxycarbonylbenzenesulfonyl)glycineamide in 40 ml. of dimethylformamide maintained under a nitrogen atmosphere is added portionwise 960 mg. (0.02 mole) of a 50%, sodium hydridesuspension in oil, and the action mixture heated at steam bath temperatures for 6 hrs. The mixture is cooled, poured into ice and water and acidified with 6N hydrochloric acid. The product is extracted with chloroform and the combined chloroformextracts (3) are back-washed with water and dried over sodium sulfate. The solvent is removed under reduced pressure and the residue gum induced to crystallize by trituration with cold isopropanol. The filtered product proves to be identical with thatreported in U.S. Pat. No. 3,591,584.
EXAMPLE 3
N-(6-Methyl-2-pyridyl)-3,4-dihydro-2-methyl-4-oxo-2H-1,2-benzothiazine-3-ca rboxamide 1,1-dioxide
In a manner similar to Examples 1 and 2, 2.03 g. (5 m moles) of N-(6-methyl-2-pyridyl)-N'-methyl-N'-(2'-propoxycarbonylbenzenesulfonyl)gly cineamide in 25 ml. of dioxane is treated with 205 mg. (5 m moles) calcium hydride and the resultingmixture heated under reflux overnight. The cooled reaction mixture is quenched in ice, acidified, and the product extracted with methylene chloride. The organic extracts are combined, dried over sodium sulfate and concentrated in vacuo to a gum. Trituration with cold acetonitrile followed by filtration provides the desired product.
EXAMPLE 4
3'-Chloro-3,4-dihydro-2-methyl-4-oxo-2H-1,2-benzothiazine-3-carboxanilide 1,1-dioxide
The procedure of Example 1 is repeated, starting with 4.11 g. (0.01 mole) of N-(3-chlorophenyl)-N'-methyl-N'-(2-methoxycarbonylbenzenesulfonyl)glyci neamide and 800 mg. (0.02 mole) of a 50 percent suspension of potassium hydride in 40 ml. ofdimethylsulfoxide, to yield the desired crude product. Further purification is achieved by recrystallization from acetic acid.
EXAMPLE 5
The procedure of Example 1 is again repeated, starting with the appropriate N-aryl-N'-alkyl-N'-(2-methoxycarbonylbenzenesulfonyl)glycineamides to provide the following congeners:
______________________________________ ##STR6## X R.sub.1 R.sub.2 ______________________________________ 6-F C.sub.6 H.sub.5 CH.sub.3 6-F 3-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 6-F 4-CH.sub.3 OC.sub.6 H.sub.4 C.sub.2 H.sub.5 8-F 4-CH.sub.3OC.sub.6 H.sub.4 CH.sub.3 8-F 4-ClC.sub.6 H.sub.4 C.sub.2 H.sub.5 8-F 6-CH.sub.32-C.sub.5 H.sub.3 N n-C.sub.3 H.sub.7 6-Cl 3-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 6-Cl 2-C.sub.3 H.sub.2 NS n-C.sub.3 H.sub.7 6-Cl 3-FC.sub.6 H.sub.4 i-C.sub.3 H.sub.7 6-Cl 2-CH.sub.3 OC.sub.6 H.sub.4 i-C.sub.3 H.sub.7 7-Cl 2-C.sub.3 H.sub.2 NS CH.sub.3 7-Cl 2-C.sub.3 H.sub.2 NS C.sub.2 H.sub.5 7-Cl 2-C.sub.5 H.sub.4 N C.sub.2 H.sub.5 7-Cl 2-C.sub.5 H.sub.4 N i-C.sub.3 H.sub.7 7-Cl 2-C.sub.4 H.sub.3 O CH.sub.3 8-Cl C.sub.6 H.sub.5 CH.sub.3 5-CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 5-CH.sub.3 4,5-(CH.sub.3).sub.2 C.sub.3 NS CH.sub.3 5-CH.sub.3 4,5-(CH.sub.3).sub.2 C.sub.3 NS n-C.sub.3 H.sub.7 5-CH.sub.3 4-ClC.sub.6 H.sub.4 C.sub.2 H.sub.5 7-Cl5-CH.sub.33-C.sub.3 HNO CH.sub.3 5-CH.sub.3 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 6-CH.sub.3 2-C.sub.3 H.sub.2 NS CH.sub.3 6-CH.sub.3 2-C.sub.5 H.sub.4 N C.sub.2 H.sub.5 6-CH.sub.3 2-C.sub.4 H.sub.3 O CH.sub.3 6-CH.sub.3 4-CH.sub.3 OC.sub.6H.sub.4 CH.sub.3 6-CH.sub.3 2-C.sub.5 H.sub.4 N i-C.sub.3 H.sub.7 7-CH.sub.3 6-CH.sub.32-C.sub. 5 H.sub.3 N CH.sub.3 7-CH.sub.3 6-CH.sub.32-C.sub. 5 H.sub.3 N n-C.sub.3 H.sub.7 7-CH.sub.3 3-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 7-CH.sub.34,5-(CH.sub.3).sub.2 C.sub.3 NS CH.sub.3 7-CH.sub.3 C.sub.6 H.sub.5 C.sub.2 H.sub.5 6-CH.sub.3 O C.sub.6 H.sub.5 CH.sub.3 6-CH.sub.3 O C.sub.6 H.sub.5 C.sub.2 H.sub.5 6-CH.sub.3 O C.sub.6 H.sub.5 n-C.sub.3 H.sub.7 6-CH.sub.3 O 2-ClC.sub.6H.sub.4 CH.sub.3 6-CH.sub.3 O 2-C.sub.4 H.sub.3 O CH.sub.3 7-CH.sub.3 O 3-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 7-CH.sub.3 O 2-C.sub.3 H.sub.2 NS n-C.sub.3 H.sub.7 7-CH.sub.3 O 2-C.sub.5 H.sub.4 N C.sub.2 H.sub.5 7-CH.sub.3 O 6-CH.sub.32-C.sub. 5H.sub.3 N CH.sub.3 7-CH.sub.3 O 3-ClC.sub.6 H.sub.4 CH.sub.3 8-CH.sub.3 O C.sub.6 H.sub.5 CH.sub.3 8-CH.sub.3 O C.sub.6 H.sub.5 C.sub.2 H.sub.5 8-CH.sub.3 O 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 8-CH.sub.3 O 4-ClC.sub.6 H.sub.4 CH.sub.3 6-CH.sub.3 5-CH.sub.33-C.sub.3 HNO CH.sub.3 6-CH.sub.3 O 5-CH.sub.33-C.sub.3 HNO CH.sub.3 ______________________________________
EXAMPLE 6
Starting with the requisite N-aryl-N'-alkyl-N'-(2-methoxycarbonylbenzenesulfonyl)glycineamide and the indicated metal hydride, the procedure of Example 2 is repeated wherein the following compounds are synthesized (product, metal hydride):
3'-methyl-3,4-dihydro-2-methyl-4-oxo-2H-1,2-benzothiazine-3-carboxanilide 1,1-dioxide, LiH; 4'-methoxy-3,4-dihydro-2-ethyl-4-oxo-2H-1,2-benzothiazine-3-carboxanilide 1,1-dioxide, CaH.sub.2 ;4'-chloro-3,4-dihydro-2-ethyl-4-oxo-2H-1,2-benzothiazine-3-carboxanilide 1,1-dioxide, KH; N-(6-methyl-2-pyridyl)-3,4-dihydro-2-n-propyl-4-oxo-2H-1,2-benzothiazine-3 -carboxamide 1,1-dioxide, NaH;2'-fluoro-3,4-dihydro-2-methyl-4-oxo-2H-1,2-benzothiazine-3-carboxanilide 1,1-dioxide, RbH; 4'-fluoro-3,4-dihydro-2-ethyl-4-oxo-2H-1,2-benzothiazine-3-carboxanilide 1,1-dioxide, CaH.sub.2 ;N-(2-thiazolyl)-3,4-dihydro-2-i-propyl-4-oxo-2H-1,2-benzothiazine-3-carbox amide 1,1-dioxide, CsH; N-(4,5-dimethyl-2-thiazolyl)-3,4-dihydro-2-methyl-4-oxo-2H1,2-benzothiazin e-3-carboxamide 1,1-dioxide, BaH.sub.2 ;N-(2-furyl)-3,4-dihydro-2-methyl-4-oxo-2H-1,2-benzothiazine-3-carboxamide 1,1-dioxide, CaH.sub.2 ; N-(2-furyl)-3,4-dihydro-2-methyl-4-oxo-2-H-1.2-benzothiazine-3-carboxamide 1,1-dioxide, LiH;3'-methoxy-3,4-dihydro-2-n-propyl-4-oxo-2H-1,2-benzothiazine-3-carboxanili de 1,1-dioxide, KH: 2'-chloro-3,4-dihydro-2-ethyl-4-oxo-2H-1,2-benzothiazine-3-carboxanilide 1,1-dioxide, MgH.sub.2 ;N-(2-pyridyl)-3,4-dihydro-2-methyl-4-oxo-2H-1,2-benzothiazine-3-carboxamid e 1,1-dioxide, RbH: N-(6-methyl-2-pyridyl)-3,4-dihydro-2-ethyl-4-oxo-2H-1,2-benzothiazine-3-ca rboxamide 1,1-dioxide, LiH4'-methyl-3,4-dihydro-2-methyl-4-oxo-2H-1,2-benzothiazine-3-carboxanilide 1,1-dioxide, KH; N-(2-thiazolyl)-3,4-dihydro-2-i-propyl-4-oxo-2H-1,2-benzothiazine-3-carbox amide 1,1-dioxide, BaH.sub. 2 ;N-(5-methyl-3-isoxazolyl)-3,4-dihydro-2-methyl-4-oxo-2H-1,2-benzothiazine- 3-carboxamide 1,1-dioxide, CaH.sub.2 ; and N-(5-methyl-3-isoxazolyl)-3,4-dihydro-2-methyl-4-oxo-2H-1,2-benzothiazine- 3-carboxamide 1,1-dioxide, LiH.
PREPARATION A
Benzyloxycarbonylglycineamides
1. N-Methyl-N'-benzyloxycarbonyl-N-(2-thiazolyl)glycineamide
to a yellow solution of 9.44 g. (42.3 m moles) of commercially available N-benzyloxycarbonyl-N-methylglycine and 4.8 g. (48 m moles) of 2-aminothiazole in 75 ml. of dry tetrahydrofuran under a nitrogen atmosphere is added dropwise 13 g. (53 mmoles) of N-ethoxycarbonyl-2-ethoxy-1,2-dihydroquinoline in 75 ml. of the same solvent. The resulting reaction mixture is allowed to stir at room temperature for 1 hr. and is then heated under reflux for 2 hrs. The solution is cooled in ice and theresulting solids filtered and dried, 4.6 g., m.p. 203.degree.-205.degree. C.
Anal. Calc'd for C.sub.14 H.sub.15 O.sub.3 N.sub.3 S: C, 55.06; H, 4.59; N, 13.76.
Found: C, 55.02; H, 4.94; N, 13.71.
2. in a similar manner to Preparation A-1, starting with the requisite glycine derivative and aryl amine, the following benzyloxycarbonylglycineamides are synthesized as intermediates:
______________________________________ ##STR7## R.sub.1 R.sub.2 ______________________________________ C.sub.6 H.sub.5 CH.sub.3, C.sub.2 H.sub.5 and n-C.sub.3 H.sub.7 6-CH.sub.32-C.sub.5 H.sub.4 N CH.sub.3, C.sub.2 H.sub.5 and n-C.sub.3H.sub.7 3-ClC.sub.6 H.sub.4 CH.sub.3 3-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 and C.sub.2 H.sub.5 2-C.sub.4 H.sub.3 O CH.sub.3 4,5-(CH.sub.3).sub.2 C.sub.3 NS CH.sub.3 and n-C.sub.3 H.sub.7 2-ClC.sub.6 H.sub.4 CH.sub.3 and C.sub.2 H.sub.5 4-ClC.sub.6 H.sub.4 CH.sub.3 and C.sub.2 H.sub.5 2-FC.sub.6 H.sub.4 CH.sub.3 2-C.sub.5 H.sub.4 N CH.sub.3, C.sub.2 H.sub.5 and i-C.sub.3 H.sub.7 4-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 2-C.sub.3 H.sub.2 NS C.sub.2H.sub.5, n-C.sub.3 H.sub.7 and i-C.sub.3 H.sub.7 4-FC.sub.6 H.sub.4 C.sub.2 H.sub.5 3-CH.sub.3 OC.sub.6 H.sub.4 n-C.sub.3 H.sub.7 3-FC.sub.6 H.sub.4 i-C.sub.3 H.sub.7 2-CH.sub.3 OC.sub.6 H.sub.4 i-C.sub.3 H.sub.7 5-CH.sub.33-C.sub.3 HNO CH.sub.3 ______________________________________
PREPARATION B
Glycineamides
1. N'-Methyl-N-(2-thiazolyl)glycineamide (3: R.sub.1 = CH.sub.3 ; R.sub.2 = 2--C.sub.3 H.sub.2 NS)
To 5 g. of N'-methyl-N'-benzyloxycarbonyl-N-(2-thiazolyl)glycineamide under a nitrogen atmosphere is added slowly with stirring 50 ml. of a 33 percent hydrogen bromide solution in acetic acid. After the vigorous evolution of carbon dioxide hassubsided, the reaction mixture is allowed to stir at room temperature overnight. Diethyl ether (275 ml.) is added and the precipitated solids filtered and dried, 5.4 g., m.p. 242.degree.-244.degree. C., dec.
The analytical sample is recrystallized from ethanoldiethyl ether.
Anal. Calc'd for C.sub.6 H.sub.9 ON.sub.3 S.2HBr: C, 21.64; H, 3.33; N, 1262.
Found: C, 22.36; H, 3.34; N, 12.87.
The free base is generated by treatment of an aqueous solution of the hydrobromide salt with an aqueous sodium hydroxide solution, followed by extraction of the free base into a water-immiscible solvent such as benzene.
2. N'-Alkyl-N-Arylglycineamides
Starting with the requisite intermediate from Preparation A-2 and following the procedure of Preparation B-1, the following intermediate products are prepared:
______________________________________ R.sub.2 NHCH.sub.2 CONHR.sub.1 R.sub.1 R.sub.2 ______________________________________ C.sub.6 H.sub.5 CH.sub.3, C.sub.2 H.sub.5 and n-C.sub.3 H.sub.7 6-CH.sub.32-C.sub.5 H.sub.4 N CH.sub.3, C.sub.2H.sub.5 and n-C.sub.3 H.sub.7 3-ClC.sub.6 H.sub.4 CH.sub.3 3-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 and C.sub.2 H.sub.5 2-C.sub.4 H.sub.3 O CH.sub.3 4,5(CH.sub.3).sub.2 C.sub.3 NS CH.sub.3 and n-C.sub.3 H.sub.7 2-ClC.sub.6 H.sub.4 CH.sub.3 and C.sub.2 H.sub.5 4-ClC.sub.6 H.sub.4 CH.sub.3 and C.sub.2 H.sub.5 2-FC.sub.6 H.sub.4 CH.sub.3 and C.sub.2 H.sub.5 2-C.sub.5 H.sub.4 N CH.sub.3, C.sub.2 H.sub.5 and i-C.sub.3 H.sub.7 4-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 2-C.sub.3 H.sub.2 NS C.sub.2 H.sub.5, n-C.sub.3 H.sub.7 and i-C.sub.3 H.sub.7 4-FC.sub. 6 H.sub.4 C.sub.2 H.sub.5 3-CH.sub.3 OC.sub.6 H.sub.4 n-C.sub.3 H.sub.7 3-FC.sub.6 H.sub.4 i-C.sub.3 H.sub.7 2-CH.sub.3 OC.sub.6 H.sub.4 i-C.sub.3H.sub.7 5-CH.sub.33-C.sub.3 HNO CH.sub.3 ______________________________________
PREPARATION C
2-Carboalkoxybenzenesulfonyl Chlorides
1. A heavy precipitate resulting from the addition of 85 ml. of 12N hydrochloric acid to 37.8 g. of methyl anthranilate in 50 ml. of cold water is stirred and maintained at 0.degree.-5.degree. C. in an ice bath while 19.0 g. of sodium nitritein 30 ml. of cold water is added dropwise. The resulting pale yellow soltuion is stirred for 30 min. at 0.degree.-5.degree. C, and is filtered through a sentered glass filter.
The above filtrate containing the diazonium salt is slowly added dropwise to a solution resulting from the addition of a cold solution of 40 g. of sulfur dioxide in 200 ml. of glacial acetic acid to a cold suspension of 8 g. of cupric chloridein 111 ml. of glacial acetic acid. During the second half of the addition and for 20 min. after the addition is complete, gas evolution is evident. After stirring the reaction mixture for 1 hr. in the cold, 1.4 l. of ice water is added and theprecipitate intermediate product is filtered and dried in vacuo, 9.2 g., m.p. 60.degree.-62.degree. C.
Meerwein, et al., Chem. Ber., 90, 841 (1957) reports a m.p. of 64.degree.-65.degree. C. for this compound which is prepared by a similar procedure.
2. Substituted 2-Carboalkoxybenzenesulfonyl chlorides
Starting with the appropriately substituted anthranilic acid esters which are either known in the chemical literature or readily prepared by methods known to those skilled in the art and employing the procedure of Meerwein, et al. or that ofPreparation C-1, the following sulfonyl chlorides are synthesized:
______________________________________ ##STR8## X R.sub.3 ______________________________________ 4-F CH.sub.3 6-F CH.sub.3 4-Cl CH.sub.3 5-Cl CH.sub.3 6-Cl CH.sub.3 3-CH.sub.3 CH.sub.3 4-CH.sub.3 CH.sub.3 5-CH.sub.3 CH.sub.3 4-CH.sub.3O CH.sub.3 5-CH.sub.3 O CH.sub.3 6-CH.sub.3 O CH.sub.3 H C.sub.2 H.sub.5 H n-C.sub.3 H.sub.7 ______________________________________
PREPARATION D
N-Benzenesulfonylglycineamides
1. N-(2-Thiazolyl)-N'-methyl-N'-(2'-methoxycarbonylbenzenesulfonyl)glycineami de
N'-Methyl-N-(2-thiazolyl)glycinemide, generated from 4.84 g. of the corresponding dihydrobromide salt, in 50 ml. of benzene is treated with 3.41 g. of 2-methoxycarbonylbenzenesulfonyl chloride, and the resulting mixture heated under reflux for30 hrs. The reaction mixture is cooled and the precipitated solids filtered, washed with benzene and partitioned between water and chloroform. The water layer is extracted several additional times with chloroform, and the chloroform extracts combinedand dried over sodium sulfate. The organic solvent is removed in vacuo and the tan residual solid is triturated with hexane and filtered, 640 mg., m.p. 215.degree. C. dec. The analytical sample is recrystallized from methanol, m.p. 216.degree.-218.degree. C. dec.
Anal. Calc'd for C.sub.14 H.sub.15 O.sub.5 N.sub.3 S.sub.2 : C, 45.52; H, 4.09; N, 11.37.
Found: C, 45.02; H, 4.12; N, 11.71.
2. n-aryl-N'-alkyl-(2'-alkoxycarbonylbenzenesulfonyl)glycineamides
Starting with the requisite intermediates from Preparations B and C and employing the procedure of Preparation D-1, the following intermediates are prepared:
______________________________________ ##STR9## X R.sub.1 R.sub.2 R.sub.3 ______________________________________ H C.sub.6 H.sub.5 CH.sub.3 C.sub.2 H.sub.5 H 6-CH.sub.32-C.sub.5 H.sub.3 N CH.sub.3 n-C.sub.3 H.sub.7 H 3-ClC.sub.6 H.sub.4 CH.sub.3 CH.sub.3 4-F C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 4-F 3-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 CH.sub.3 4-F 4-CH.sub.3 OC.sub.6 H.sub.4 C.sub.2 H.sub.5 CH.sub.3 6-F 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 CH.sub.3 6-F 4-ClC.sub.6 H.sub.4 C.sub.2H.sub.5 CH.sub.3 6-F 6-CH.sub.3 -2-C.sub. 5 H.sub.3 N n-C.sub.3 H.sub.7 CH.sub.3 4-Cl 3-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 CH.sub.3 4-Cl 2-C.sub.3 H.sub.2 NS n-C.sub.3 H.sub. 7 CH.sub.3 4-Cl 3-FC.sub.6 H.sub.4 i-C.sub.3 H.sub.7 CH.sub.3 4-Cl2-CH.sub.3 OC.sub.6 H.sub.4 i-C.sub.3 H.sub.7 CH.sub.3 5-Cl 2-C.sub.3 H.sub.2 NS CH.sub.3 CH.sub.3 5-Cl 2-C.sub.3 H.sub.2 NS C.sub.2 H.sub.5 CH.sub.3 5-Cl 2-C.sub.5 H.sub.4 N C.sub.2 H.sub.5 CH.sub.3 5-Cl 2-C.sub.5 H.sub.4 N i-C.sub.3 H.sub.7 CH.sub.3 5-Cl 2-C.sub.4 H.sub.3 O CH.sub.3 CH.sub.3 6-Cl C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 3-CH.sub.3 C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 3-CH.sub.3 4,5-(CH.sub.3).sub.2 -2-C.sub.3 NS CH.sub.3 CH.sub.3 3-CH.sub.3 4,5-(CH.sub.3).sub.2 -2-C.sub.3NS n-C.sub.3 H.sub.7 CH.sub.3 3-CH.sub.3 4-ClC.sub.6 H.sub.4 C.sub.2 H.sub.5 CH.sub.3 3-CH.sub.3 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 CH.sub.3 4-CH.sub.3 2-C.sub.3 H.sub.2 NS CH.sub.3 CH.sub.3 4-CH.sub.3 2-C.sub.5 H.sub.4 N C.sub.2 H.sub.5 CH.sub.3 4-CH.sub.3 2-C.sub.4 H.sub.3 O CH.sub.3 CH.sub.3 4-CH.sub.3 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 CH.sub.3 4-CH.sub.3 2-C.sub.5 H.sub.4 N i-C.sub.3 H.sub.7 CH.sub.3 5-CH.sub.3 6-CH.sub.3 -2-C.sub.5 H.sub.3 N CH.sub.3 CH.sub.3 5-CH.sub.3 6-CH.sub.3 -2-C.sub.5 H.sub.3 N n-C.sub.3 H.sub.7 CH.sub.3 5-CH.sub.3 3-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 CH.sub.3 5-CH.sub.3 4,5-(CH.sub.3).sub.2 C.sub.3 NS CH.sub.3 CH.sub.3 5-CH.sub.3 C.sub.6 H.sub.5 C.sub.2 H.sub.5 CH.sub.3 4-CH.sub.3 O C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 4-CH.sub.3 O C.sub.6 H.sub.5 C.sub.2 H.sub.5 CH.sub.3 4-CH.sub.3 O C.sub.6 H.sub.5 n-C.sub.3 H.sub.7 CH.sub.3 4-CH.sub.3 O 2-ClC.sub.6 H.sub.4 CH.sub.3 CH.sub.3 4-CH.sub.3 O 2-C.sub.4 H.sub.3 O CH.sub.3 CH.sub.3 5-CH.sub.3 O 3-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 CH.sub.3 5-CH.sub.3 O 2-C.sub.3 H.sub.2 NS n-C.sub.3 H.sub.7 CH.sub.3 5-CH.sub.3 O 2-C.sub.3 H.sub.4 N C.sub.2 H.sub.5 CH.sub.3 5-CH.sub.3 O 6-CH.sub.3 -2-C.sub. 5 H.sub.3 N CH.sub.3 CH.sub.3 5-CH.sub.3 O 3-CLC.sub.6 H.sub.4 CH.sub.3 CH.sub.3 6-CH.sub.3 O C.sub.6 H.sub.5 CH.sub.3 CH.sub.3 6-CH.sub.3 O C.sub.6 H.sub.5 C.sub.2 H.sub.5 CH.sub.3 6-CH.sub.3 O 4-CH.sub.3 OC.sub.6 H.sub.4 CH.sub.3 CH.sub.3 6-CH.sub.3 O 4-ClC.sub.6 H.sub.4 CH.sub.3 CH.sub.3 H 3-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 CH.sub.3 H 4-CH.sub.3 OC.sub.6 H.sub.4 C.sub.2 H.sub.5 CH.sub.3 5-Cl 5-CH.sub.3 -3-C.sub.3 HNO CH.sub.3 CH.sub.3 4-CH.sub.3 5-CH.sub.3 -3-C.sub.3 HNO CH.sub.3 CH.sub.3 4-CH.sub.3 O 5-CH.sub.3 -3-C.sub.3 HNO CH.sub.3 CH.sub.3 H 5-CH.sub.3 -3-C.sub.3 HNO CH.sub.3 CH.sub.3 H 4-ClC.sub.6 H.sub. 4 C.sub.2 H.sub.5 CH.sub.3 H 6-CH.sub.32-C.sub.5 H.sub.3 N n-C.sub.3 H.sub.7 CH.sub.3 H 2-FC.sub.6 H.sub.4 CH.sub.3CH.sub.3 H 4-FC.sub.6 H.sub.4 C.sub.2 H.sub.5 CH.sub.3 H 2-C.sub.3 H.sub.2 NS i-C.sub.3 H.sub.7 CH.sub.3 H 4,5-(CH.sub.3).sub.22-C.sub. 3 NS CH.sub.3 CH.sub.3 H 2-C.sub.4 H.sub.3 O CH.sub.3 CH.sub.3 H 3-CH.sub.3 OC.sub.6 H.sub.4 n-C.sub.3H.sub.7 CH.sub.3 H 2-ClC.sub.6 H.sub.4 C.sub.2 H.sub.5 CH.sub.3 H 2-C.sub.5 H.sub.4 N CH.sub.3 CH.sub.3 H 6-CH.sub.32-C.sub.5 H.sub.3 N C.sub.2 H.sub.5 CH.sub.3 H 4-CH.sub.3 C.sub.6 H.sub.4 CH.sub.3 CH.sub.3 ______________________________________
PREPARATION E
Metal Hydrides
The metal hydrides utilized in the present process are either commercially available or are prepared by literature procedures, Moeller, "Inorganic Chemistry," John Wiley & Sons, New York, New York 1959.
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