Bromide ion → N-[2-(3-methoxy-4-prop-2-ynyloxy-phenyl)-ethyl]-3-phenyl-2-prop-2-ynyloxy-butyramide
Reaction equation
[Br-:41].[CH2:1]([C:2]#[CH:3])[Br:4].[CH3:42][CH2:43][CH2:44][CH2:45][N+:46]([CH2:47][CH2:48][CH2:49][CH3:50])([CH2:51][CH2:52][CH2:53][CH3:54])[CH2:55][CH2:56][CH2:57][CH3:58].[CH3:5][c:6]1[cH:7][cH:8][cH:9][cH:10][cH:11]1.[Cl:59][CH2:60][Cl:61].[Na+:40].[OH-:39].[OH:12][CH:13]([C:14](=[O:15])[NH:16][CH2:17][CH2:18][c:19]1[cH:20][c:21]([O:29][CH3:30])[c:22]([O:25][CH2:26][C:27]#[CH:28])[cH:23][cH:24]1)[CH:31]([CH3:32])[c:33]1[cH:34][cH:35][cH:36][cH:37][cH:38]1>>[CH:1]#[C:2][CH2:3][O:12][CH:13]([C:14](=[O:15])[NH:16][CH2:17][CH2:18][c:19]1[cH:20][c:21]([O:29][CH3:30])[c:22]([O:25][CH2:26][C:27]#[CH:28])[cH:23][cH:24]1)[CH:31]([CH3:32])[c:33]1[cH:34][cH:35][cH:36][cH:37][cH:38]1Participants
9
Reactant 8
Product 1
Sources & evidence
- ORD record
- ord-9b5cf126d3244ab0a5278b9178b6fbe2
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (3/10)
Reaction notes
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