Hydrochloric Acid → N-(5-dimethylsilyloxy-2,6,6-trimethylhept-3-yn-2-yl)-2-quinolin-6-yloxybutanamide
Reaction equation
[C:45]([O:46][CH2:47][CH3:48])(=[O:49])[CH3:50].[CH3:34][N:35]([CH3:36])[CH2:37][CH2:38][CH2:39][N:40]=[C:41]=[N:42][CH2:43][CH3:44].[CH3:51][CH2:52][CH2:53][CH2:54][CH2:55][CH3:56].[CH3:57][N:58]([CH3:59])[c:60]1[cH:61][cH:62][n:63][cH:64][cH:65]1.[CH3:69][CH2:70][CH2:71][CH2:72][CH2:73][CH3:74].[Cl:66][CH2:67][Cl:68].[ClH:33].[NH2:18][C:19]([C:20]#[C:21][CH:22]([C:23]([CH3:24])([CH3:25])[CH3:26])[O:27][SiH:28]([CH3:29])[CH3:30])([CH3:31])[CH3:32].[n:1]1[cH:2][cH:3][cH:4][c:5]2[cH:6][c:7]([O:11][CH:12]([C:13](=[O:14])[OH:15])[CH2:16][CH3:17])[cH:8][cH:9][c:10]12>>[n:1]1[cH:2][cH:3][cH:4][c:5]2[cH:6][c:7]([O:11][CH:12]([C:13](=[O:15])[NH:18][C:19]([C:20]#[C:21][CH:22]([C:23]([CH3:24])([CH3:25])[CH3:26])[O:27][SiH:28]([CH3:29])[CH3:30])([CH3:31])[CH3:32])[CH2:16][CH3:17])[cH:8][cH:9][c:10]12Participants
9
Reactant 8
Product 1
Sources & evidence
- ORD record
- ord-26326cc3ae764e138e9b9440974e33d5
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (1/10)
Reaction notes
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