Hydrochloric Acid → N-(2-(5-chloro-1H-indol-3-yl)ethyl)-1-(4-isopropylphenyl)-2-oxopyrrolidine-3-carboxamide
Reaction equation
[CH:48]([CH3:49])([CH3:50])[c:51]1[cH:52][cH:53][c:54]([N:57]2[C:58](=[O:65])[CH:59]([C:62](=[O:63])[OH:64])[CH2:60][CH2:61]2)[cH:55][cH:56]1.[Cl:2][c:3]1[cH:4][c:5]2[c:6]([CH2:12][CH2:13][NH2:14])[cH:7][nH:8][c:9]2[cH:10][cH:11]1.[ClH:1].[O:66]=[CH:67][N:68]([CH3:69])[CH3:70].[P-:15]([F:16])([F:17])([F:18])([F:19])([F:20])[F:21].[n:22]1([O:23][P+:24]([N:25]2[CH2:26][CH2:27][CH2:28][CH2:29]2)([N:30]2[CH2:31][CH2:32][CH2:33][CH2:34]2)[N:35]2[CH2:36][CH2:37][CH2:38][CH2:39]2)[c:40]2[cH:41][cH:42][cH:43][cH:44][c:45]2[n:46][n:47]1>>[Cl:2][c:3]1[cH:4][c:5]2[c:6]([CH2:12][CH2:13][NH:14][C:62]([CH:59]3[C:58](=[O:65])[N:57]([c:54]4[cH:53][cH:52][c:51]([CH:48]([CH3:49])[CH3:50])[cH:56][cH:55]4)[CH2:61][CH2:60]3)=[O:63])[cH:7][nH:8][c:9]2[cH:10][cH:11]1Participants
7
Reactant 6
Product 1
Sources & evidence
- ORD record
- ord-cb467c252a444150998e0bbcb15966c5
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (7/10)
Reaction notes
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