Hydrochloric Acid → 5-(6-(5-hydroxyindoline-1-carbonyl)pyrimidin-4-ylamino)-1,3-dihydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-2'(1'H)-one
Reaction equation
[B-:40]([F:41])([F:42])([F:43])[F:44].[ClH:1].[NH:30]1[CH2:31][CH2:32][c:33]2[cH:34][c:35]([OH:39])[cH:36][cH:37][c:38]21.[O:2]=[C:3]1[NH:4][c:5]2[n:6][cH:7][cH:8][cH:9][c:10]2[C:11]12[CH2:12][c:13]1[cH:14][cH:15][c:16]([NH:20][c:21]3[cH:22][c:23]([C:27](=[O:28])[OH:29])[n:24][cH:25][n:26]3)[cH:17][c:18]1[CH2:19]2.[O:62]=[CH:63][N:64]([CH3:65])[CH3:66].[n:45]1([O:46][C:47]([N:48]([CH3:49])[CH3:50])=[N+:51]([CH3:52])[CH3:53])[c:54]2[cH:55][cH:56][cH:57][cH:58][c:59]2[n:60][n:61]1>>[O:2]=[C:3]1[NH:4][c:5]2[n:6][cH:7][cH:8][cH:9][c:10]2[C:11]12[CH2:12][c:13]1[cH:14][cH:15][c:16]([NH:20][c:21]3[cH:22][c:23]([C:27](=[O:28])[N:30]4[CH2:31][CH2:32][c:33]5[cH:34][c:35]([OH:39])[cH:36][cH:37][c:38]54)[n:24][cH:25][n:26]3)[cH:17][c:18]1[CH2:19]2Participants
7
Reactant 6
Product 1
Sources & evidence
- ORD record
- ord-a4b303ccfaaf41d29be977c09707508d
- Source dataset
- Training data from https://doi.org/10.1039/C8SC04228D (4/10)
Reaction notes
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