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机构地区:[1]DepartmentofMedicinalChemistry,InsituteofMateriaMedica,ChineseAcademyofMedicalScience&PekingUnionMedicalCollege,Beijing100050 [2]DepartmentofMedicinalChemistry,InsituteofMateriaMedica,ChineseAcademyofMed
出 处:《Chinese Chemical Letters》2002年第5期412-415,共4页中国化学快报(英文版)
摘 要:A series of 3-methoxycarbonylpropoxy-7-(imidazol-4-ylpropinamide)-1, 3-dihydrogen- 1-methyl-5-phenyl-2H-1, 4-benzodiazepin-2-ones, as farnesyltransferase(Ftase) inhibitors, were synthesized. The preparation of the key intermediate, 7-amino-3-methoxycabonylpropoxy-1- methyl-5-phenyl-2H-1,4-benzodiazepin-2-one, was improved.A series of 3-methoxycarbonylpropoxy-7-(imidazol-4-ylpropinamide)-1, 3-dihydrogen- 1-methyl-5-phenyl-2H-1, 4-benzodiazepin-2-ones, as farnesyltransferase(Ftase) inhibitors, were synthesized. The preparation of the key intermediate, 7-amino-3-methoxycabonylpropoxy-1- methyl-5-phenyl-2H-1,4-benzodiazepin-2-one, was improved.
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