Hydrochloric Acid → 2-(5-chloro-3-pyridyloxy)-N-(1-tert.butyldimethylsilyloxy-4-methylpent-2-yn-4-yl)butyramide
Reaction equation
[CH3:31][N:32]([CH2:33][CH2:34][CH2:35][N:36]=[C:37]=[N:38][CH2:39][CH3:40])[CH3:41].[CH3:42][N:43]([CH3:44])[c:45]1[cH:46][cH:47][n:48][cH:49][cH:50]1.[Cl:1][c:2]1[cH:3][c:4]([O:8][CH:9]([C:10](=[O:11])[OH:12])[CH2:13][CH3:14])[cH:5][n:6][cH:7]1.[Cl:51][CH2:52][Cl:53].[ClH:30].[NH2:15][C:16]([C:17]#[C:18][CH:19]([C:20]([CH3:21])([CH3:22])[CH3:23])[O:24][SiH:25]([CH3:26])[CH3:27])([CH3:28])[CH3:29]>>[Cl:1][c:2]1[cH:3][c:4]([O:8][CH:9]([C:10](=[O:12])[NH:15][C:16]([C:17]#[C:18][CH:19]([C:20]([CH3:21])([CH3:22])[CH3:23])[O:24][SiH:25]([CH3:26])[CH3:27])([CH3:28])[CH3:29])[CH2:13][CH3:14])[cH:5][n:6][cH:7]1Participants
7
Reactant 6
Product 1
Sources & evidence
- ORD record
- ord-a5fe341c3e114dca94c398a6873bc334
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (8/10)
Reaction notes
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