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HCID 59619632, compound → HCID 59619767, compound

HRID 298126
Notes
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Reaction equation

HRID 298126 reaction equation
[Br:1][c:2]1[cH:3][c:4]2[c:5]3[c:6]([cH:7][n:8][c:9]2[cH:10][cH:11]1)[n:12]([CH3:23])[c:13](=[O:22])[n:14]3-[c:15]1[c:16]([CH3:21])[n:17][n:18]([CH3:20])[cH:19]1.[F:24][CH2:25][CH2:26][O:27][c:28]1[cH:29][n:30][cH:31][c:32]([B:34]2[O:35][C:36]([CH3:37])([CH3:38])[C:39]([CH3:40])([CH3:41])[O:42]2)[cH:33]1>>[c:2]1(-[c:32]2[cH:31][n:30][cH:29][c:28]([O:27][CH2:26][CH2:25][F:24])[cH:33]2)[cH:3][c:4]2[c:5]3[c:6]([cH:7][n:8][c:9]2[cH:10][cH:11]1)[n:12]([CH3:23])[c:13](=[O:22])[n:14]3-[c:15]1[c:16]([CH3:21])[n:17][n:18]([CH3:20])[cH:19]1
ParticipantsSources & evidenceReaction notes

Participants

3

Reactant 2

HCID 59619632HCID 59619632, compoundHCID 596197398-Bromo-1-(1,3-dimethyl-1H-pyrazol-4-yl)-3-methyl-1,3-dihydro-imidazo[4,5-c]quinolin-2-one

Product 1

HCID 59619767HCID 59619767, compound

Sources & evidence

ORD record
ord-417835c607784b6499fbace38b0b5ac9
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)
DOI
10.1039/C8SC04228D

Reaction notes

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On this pageParticipantsSources & evidenceReaction notes