6-(6,7-Dimethoxyquinazolin-4-yloxy)-1-naphthoic acid → HCID 49805504, compound
Reaction equation
[CH3:1][O:2][c:3]1[cH:4][c:5]2[c:6]([O:15][c:16]3[cH:17][c:18]4[cH:19][cH:20][cH:21][c:22]([C:26](=[O:27])[OH:28])[c:23]4[cH:24][cH:25]3)[n:7][cH:8][n:9][c:10]2[cH:11][c:12]1[O:13][CH3:14].[NH2:29][CH2:30][c:31]1[cH:32][cH:33][c:34]([C:35](=[O:36])[NH:37][c:38]2[c:39]([NH2:46])[cH:40][c:41]([O:44][CH3:45])[cH:42][cH:43]2)[cH:47][cH:48]1>>[CH3:1][O:2][c:3]1[cH:4][c:5]2[c:6]([O:15][c:16]3[cH:17][c:18]4[cH:19][cH:20][cH:21][c:22]([C:26](=[O:27])[NH:29][CH2:30][c:31]5[cH:32][cH:33][c:34]([C:35](=[O:36])[NH:37][c:38]6[c:39]([NH2:46])[cH:40][c:41]([O:44][CH3:45])[cH:42][cH:43]6)[cH:47][cH:48]5)[c:23]4[cH:24][cH:25]3)[n:7][cH:8][n:9][c:10]2[cH:11][c:12]1[O:13][CH3:14]Participants
3
Sources & evidence
- ORD record
- ord-0d0af4197ae04933b43caa98a7cbcb22
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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