【结 构 式】 |
【分子编号】50129 【品名】methyl 1-methyl-2,3-dihydro-1H-1,4-benzodiazepin-5-yl sulfide; 1-methyl-5-(methylsulfanyl)-2,3-dihydro-1H-1,4-benzodiazepine 【CA登记号】 |
【 分 子 式 】C11H14N2S 【 分 子 量 】206.31164 【元素组成】C 64.04% H 6.84% N 13.58% S 15.54% |
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:(I)The known (methylmercapto)benzodiazepine (I) was condensed with isonicotinic hydrazide (II) in refluxing EtOH to give the intermediate hydrazinobenzodiazepine (III), which under the reaction conditions cyclized to the target triazolobenzodiazepine.
【1】 Vega, S.; Madronero, R.; Synthesis of triazolo[4,3-d]-, tetrazolo[1,5-a]- and quinazolino[3,2-d] [1,4]benzodiazepines. J Heterocycl Chem 1978, 15, 7, 1127. |
中间体序号 | 中间体编号 | 品名 | CAS号 | 分子式 | 供应商 | 用于合成 |
---|---|---|---|---|---|---|
(I) | 50129 | methyl 1-methyl-2,3-dihydro-1H-1,4-benzodiazepin-5-yl sulfide; 1-methyl-5-(methylsulfanyl)-2,3-dihydro-1H-1,4-benzodiazepine | C11H14N2S | 详情 | 详情 | |
(II) | 26079 | Isonicotinohydrazide | 54-85-3 | C6H7N3O | 详情 | 详情 |
(III) | 50130 | N'-(1-methyl-2,3-dihydro-1H-1,4-benzodiazepin-5-yl)isonicotinohydrazide | C16H17N5O | 详情 | 详情 |
Extended Information