发明授权
US5536869A Process for the preparation of ethyl
3S-[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentyn
oate
失效
制备3S- [4 - [[4-(氨基亚氨基甲基)苯基]氨基] -1,4-二氧代丁基]氨基] -4-戊酸乙酯的方法
- 专利标题: Process for the preparation of ethyl 3S-[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentyn oate
- 专利标题(中): 制备3S- [4 - [[4-(氨基亚氨基甲基)苯基]氨基] -1,4-二氧代丁基]氨基] -4-戊酸乙酯的方法
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申请号: US502054申请日: 1995-07-14
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公开(公告)号: US5536869A公开(公告)日: 1996-07-16
- 发明人: Kevin A. Babiak , Srinivasan Babu , James R. Behling , Mark L. Boys , Kimberly J. Cain-Janicki , Wendel W. Doubleday , Payman Farid , Timothy J. Hagen , E. Ann Hallinan , Donald W. Hansen, Jr. , Donald E. Korte , Kathleen T. McLaughlin , John R. Medich , Sean T. Nugent , Vlasdislav Orlovski , Jung M. Park , Karen B. Peterson , Daniel R. Pilipauskas , Barnett S. Pitzele , Sofya Tsymbalov , Glenn L. Stahl
- 申请人: Kevin A. Babiak , Srinivasan Babu , James R. Behling , Mark L. Boys , Kimberly J. Cain-Janicki , Wendel W. Doubleday , Payman Farid , Timothy J. Hagen , E. Ann Hallinan , Donald W. Hansen, Jr. , Donald E. Korte , Kathleen T. McLaughlin , John R. Medich , Sean T. Nugent , Vlasdislav Orlovski , Jung M. Park , Karen B. Peterson , Daniel R. Pilipauskas , Barnett S. Pitzele , Sofya Tsymbalov , Glenn L. Stahl
- 申请人地址: IL Chicago
- 专利权人: G. D. Searle & Co.
- 当前专利权人: G. D. Searle & Co.
- 当前专利权人地址: IL Chicago
- 主分类号: C07C227/02
- IPC分类号: C07C227/02 ; C07B61/00 ; C07C227/12 ; C07C227/34 ; C07C229/08 ; C07C257/18 ; C07C229/24
摘要:
The present invention relates to a novel process for the preparation of ethyl 3S-[[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentynoate and pharmaceutically acceptable acid addition salt thereof which comprises treating (trimethylsilyl)acetylene sequentially with n-butyllithium and 4-formylmorpholine followed by acid hydrolysis to give 3-(trimethylsilyl)-2-propynal; treating 3-(trimethylsilyl)-2-propynal with lithium bis(trimethylsilyl)amide to give in situ N,3-bis(trimethylsilyl)-2-propyn-1-imine; condensation of N,3-bis(trimethylsilyl)-2-propyn-1-imine with lithium t-butyl acetate to give (.+-.)1,1-dimethylethyl 3-amino-5-(trimethylsilyl)-4-pentynoate; treating (.+-.)1,1-dimethylethyl 3-amino-5-(trimethylsilyl)-4-pentynoate- with p-toluenesulfonic acid to give (.+-.)1,1-dimethylethyl 3-amino-5-(trimethylsilyl)-4-pentynoate, mono p-toluenesulfonic acid salt, treatment of resulting salt with ethanol in the presence of p-toluenesulfonic acid to give (.+-.)ethyl 3-amino-5-(trimethylsilyl)-4-pentynoate; desilylation of (.+-.)ethyl 3-amino-5-(trimethylsilyl)-4-pentynoate to give in situ (.+-.)ethyl 3-amino-4-pentynoate; resolution of (.+-.)ethyl 3-amino-4-pentynoate using (R)-(-)-mandelic acid and treatment of the resolved product with gaseous hydrochloric acid to give ethyl 3S-amino-4-pentynoate, monohydrochloride; coupling the ethyl 3S-amino-4-pentynoate, monohydrochloride to 4-[[4-(aminoiminomethyl)phenyl]amino]-4-oxobutanoic acid, monohydrochloride in the presence of isobutyl chloroformate and N-methylmorpholine to give ethyl 3S-[[4-[[4-(aminoiminomethyl)phenyl]amino]-1,4-dioxobutyl]amino]-4-pentynoate, monohydrochloride.
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