HCID 59619738, compound → HCID 59619932, compound

HRID 2338210Notes

Reaction equation

HRID 2338210 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.[CH:24]([CH3:25])([CH3:26])[O:27][c:28]1[c:29]([CH2:43][OH:44])[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][c:29]([CH2:43][OH:44])[c:28]([O:27][CH:24]([CH3:25])[CH3:26])[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

Participants

3

Reactant 2

HCID 59619738HCID 59619738, 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 59619932HCID 59619932, compound

Sources & evidence

ORD record
ord-7b64aeafe7e94a539121b818eebc3ea9
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (10/10)

Reaction notes

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