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【结 构 式】

【分子编号】33975

【品名】7-chloro-1-methyl-5-phenyl-1,3,4,5-tetrahydro-2H-1,4-benzodiazepin-2-one

【CA登记号】

【 分 子 式 】C16H15ClN2O

【 分 子 量 】286.76068

【元素组成】C 67.02% H 5.27% Cl 12.36% N 9.77% O 5.58%

与该中间体有关的原料药合成路线共 1 条

合成路线1

该中间体在本合成路线中的序号:(V)

The methylation of 2-amino-5-chlorobenzophenone (I) with dimethyl-sulfate affords the 5-chloro-2-methylaminobenzophenone (II), which is conden-sed with bromoacetyl bromide (A) to yieId 2-(2-bromo-N-methylacetamido)-5-chlorobenzophenone (III). The amonolysis of (III) with ammonia in methanol gives 2-(2-amino-N-methylacetamido)-5-chlorobenzophenone (IV), which is finally condensed with diketene (B) in refluxing acetone. This product can also be obtained by condensation of 7-chloro-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one (V) with acetyl chloride (C) and triethylamine in ether or with diketene (B) in acetone.

1 Szmuszkovicz, J.; et al.; Tetrahedron Lett 1971, 39, 39, 3665.
2 Szmuszkovicz, J.; Oxazinobenzodiazepine derivatives. DE 1947226; ES 371392; FR 2018432; GB 1222294 .
3 Szmuszkovicz, J.; Process for the preparation of 11-chloro-8,12b-dihydro-2,8-dimethyl-12b-phenyl-4H-[1,3]oxazino[3,2-d]benzodiazepine-4,7-6H-dione. CH 530414; JP 49025953B; NL 7014824; US 3575965 .
4 Castaner, J.; Chatterjee, S.S.; Ketazolam. Drugs Fut 1976, 1, 6, 293.
中间体序号 中间体编号 品名 CAS号 分子式 供应商 用于合成
(B) 11367 4-Methylene-2-oxetanone; Acetyl ketene 674-82-8 C4H4O2 详情 详情
(A) 14005 2-Bromoacetyl bromide; Bromoacetyl bromide 598-21-0 C2H2Br2O 详情 详情
(I) 10279 (2-Amino-5-chlorophenyl)(phenyl)methanone; 2-Amino-5-chlorobenzophenone 719-59-5 C13H10ClNO 详情 详情
(II) 33972 [5-chloro-2-(methylamino)phenyl](phenyl)methanone 1022-13-5 C14H12ClNO 详情 详情
(III) 33973 N-(2-benzoyl-4-chlorophenyl)-2-bromo-N-methylacetamide C16H13BrClNO2 详情 详情
(IV) 33974 2-amino-N-(2-benzoyl-4-chlorophenyl)-N-methylacetamide C16H15ClN2O2 详情 详情
(V) 33975 7-chloro-1-methyl-5-phenyl-1,3,4,5-tetrahydro-2H-1,4-benzodiazepin-2-one C16H15ClN2O 详情 详情
(C) 19273 acetyl chloride 75-36-5 C2H3ClO 详情 详情
Extended Information