4-吡咯烷-1-基哌啶 → 6,6-Dimethyl-11-oxo-8-(4-pyrrolidin-1-yl-piperidin-1-yl)-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

HRID 61735

反应方程式

HRID 61735 反应方程式
[C:1]([C:3]1[CH:15]=[C:14]2[C:6]([C:7]3[C:8](=[O:30])[C:9]4[CH:21]=[CH:20][C:19](OS(C(F)(F)F)(=O)=O)=[CH:18][C:10]=4[C:11]([CH3:17])([CH3:16])[C:12]=3[NH:13]2)=[CH:5][CH:4]=1)#[N:2].[N:31]1([CH:36]2[CH2:41][CH2:40][NH:39][CH2:38][CH2:37]2)[CH2:35][CH2:34][CH2:33][CH2:32]1>>[CH3:16][C:11]1([CH3:17])[C:12]2[NH:13][C:14]3[C:6](=[CH:5][CH:4]=[C:3]([C:1]#[N:2])[CH:15]=3)[C:7]=2[C:8](=[O:30])[C:9]2[CH:21]=[CH:20][C:19]([N:39]3[CH2:40][CH2:41][CH:36]([N:31]4[CH2:35][CH2:34][CH2:33][CH2:32]4)[CH2:37][CH2:38]3)=[CH:18][C:10]1=2

参与物

3

反应物 2

HCID 787034-吡咯烷-1-基哌啶HCID 86663817Trifluoro-methanesulfonic acid 3-cyano-6,6-dimethyl-11-oxo-6,11-dihydro-5H-benzo[b]carbazol-8-yl ester

产物 1

HCID 498048666,6-Dimethyl-11-oxo-8-(4-pyrrolidin-1-yl-piperidin-1-yl)-6,11-dihydro-5H-benzo[b]carbazole-3-carbonitrile

实验过程

Under the same conditions as the method for synthesizing Compound B2-1, the title compound was prepared from Compound B1 and 4-pyrrolidin-1-yl-piperidine.

后处理

  1. customUnder the same conditions as the method for synthesizing Compound B2-1

来源与证据

ORD记录
ord-e7478618c39a44b9a1420668f376ae4d
来源数据集
uspto-grants-2016_09
专利号
US09440922B2

关联笔记

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