HRID1073715

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID53167

1-Methylpiperazine

C5H12N2

结构：O=C(NC1N=C(c2ccccc2)c2ccccc2N(CCBr)C1=O)c1cc2ccccc2[nH]1

HCID20097467

未命名化合物

PRODUCTS

生成物

结构：CN1CCN(CCN2C(=O)C(NC(=O)c3cc4ccccc4[nH]3)N=C(c3ccccc3)c3ccccc32)CC1

HCID14800325

未命名化合物

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID7914

Isopropyl ether

C6H14O

PROCEDURE

实验过程

A mixture of (3RS)-1,3-dihydro-3-(2-indolylcarbonylamino) -1-(2-bromoethyl)-5-phenyl-2H-1,4-benzodiazepine-2-one (0.3 g) and 1-methylpiperazine (3.0 ml) was stirred for 4.0 hours at room temperature aND diisopropyl ether (20 ml) was added thereto. The resultant precipitates were collected by filtration and dissolved in diluted hydrochloric acid. The solution was adjusted to pH 7 with an aqueous solution of sodium bicarbonate and the resultant precipitates were collected by filtration to give (3RS)-1,3-dihydro-3-(2-indolylcarbonylamino)-1-[2-(4-methyl-1-piperazinyl)ethyl]-5-phenyl-2H-1,4-benzodiazepine-2-one (0.20 g).

WORKUP

后处理

additionwas added
customThe resultant precipitates
filtrationwere collected by filtration
dissolutiondissolved in diluted hydrochloric acid
customthe resultant precipitates
filtrationwere collected by filtration

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-03b7972d32df4cadb7d0ddbd665b5fdf
来源数据集: uspto-grants-1990_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04970207
来源说明: uspto-grants-1990_11

反应 SMILES

[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10]([NH:12][CH:13]1[N:19]=[C:18]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:17]2[CH:26]=[CH:27][CH:28]=[CH:29][C:16]=2[N:15]([CH2:30][CH2:31]Br)[C:14]1=[O:33])=[O:11].[CH3:34][N:35]1[CH2:40][CH2:39][NH:38][CH2:37][CH2:36]1>C(OC(C)C)(C)C>[NH:1]1[C:9]2[C:4](=[CH:5][CH:6]=[CH:7][CH:8]=2)[CH:3]=[C:2]1[C:10]([NH:12][CH:13]1[N:19]=[C:18]([C:20]2[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=2)[C:17]2[CH:26]=[CH:27][CH:28]=[CH:29][C:16]=2[N:15]([CH2:30][CH2:31][N:38]2[CH2:39][CH2:40][N:35]([CH3:34])[CH2:36][CH2:37]2)[C:14]1=[O:33])=[O:11]