HRID960674

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID313

Hydrochloric Acid

ClH

HCID1049

Pyridine

C5H5N

HCID10797680

Tetrahydro-1H-pyrrolizine-7a(5H)-acetyl chloride

C9H14ClNO

结构：CC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCSCCN

HCID53686948

未命名化合物

PRODUCTS

生成物

结构：CC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCCC(C)=CCSCCNC(=O)CC12CCCN1CCC2

HCID54345510

未命名化合物

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-d37bbbebd0044e7e821df51346193259
来源数据集: Validation data from https://doi.org/10.1039/C8SC04228D
DOI: 10.1039/C8SC04228D
来源说明: Validation data from https://doi.org/10.1039/C8SC04228D

反应 SMILES

[CH3:14][C:15](=[CH:16][CH2:17][S:18][CH2:19][CH2:20][NH2:21])[CH2:22][CH2:23][CH:24]=[C:25]([CH2:26][CH2:27][CH:28]=[C:29]([CH2:30][CH2:31][CH:32]=[C:33]([CH2:34][CH2:35][CH:36]=[C:37]([CH2:38][CH2:39][CH:40]=[C:41]([CH2:42][CH2:43][CH:44]=[C:45]([CH2:46][CH2:47][CH:48]=[C:49]([CH2:50][CH2:51][CH:52]=[C:53]([CH2:54][CH2:55][CH:56]=[C:57]([CH3:58])[CH3:59])[CH3:60])[CH3:61])[CH3:62])[CH3:63])[CH3:64])[CH3:65])[CH3:66])[CH3:67].[ClH:1].[N:2]12[CH2:3][CH2:4][CH2:5][C:6]1([CH2:10][C:11](=[O:12])[Cl:13])[CH2:7][CH2:8][CH2:9]2.[cH:68]1[cH:69][cH:70][n:71][cH:72][cH:73]1>>[N:2]12[CH2:3][CH2:4][CH2:5][C:6]1([CH2:10][C:11](=[O:12])[NH:21][CH2:20][CH2:19][S:18][CH2:17][CH:16]=[C:15]([CH3:14])[CH2:22][CH2:23][CH:24]=[C:25]([CH2:26][CH2:27][CH:28]=[C:29]([CH2:30][CH2:31][CH:32]=[C:33]([CH2:34][CH2:35][CH:36]=[C:37]([CH2:38][CH2:39][CH:40]=[C:41]([CH2:42][CH2:43][CH:44]=[C:45]([CH2:46][CH2:47][CH:48]=[C:49]([CH2:50][CH2:51][CH:52]=[C:53]([CH2:54][CH2:55][CH:56]=[C:57]([CH3:58])[CH3:59])[CH3:60])[CH3:61])[CH3:62])[CH3:63])[CH3:64])[CH3:65])[CH3:66])[CH3:67])[CH2:7][CH2:8][CH2:9]2