Bromide ion → 1-(6-Bromo-pyridin-2-ylmethyl)-3-(4-isopropyl-benzoyl)-1H-quinolin-4-one

HRID 213568Notes

Reaction equation

HRID 213568 reaction equation
[Br-:26].[CH2:37]1[O:38][CH2:39][CH2:40][CH2:41]1.[CH3:1][O:2][N:3]([C:4](=[O:5])[c:6]1[cH:7][n:8]([CH2:17][c:18]2[n:19][c:20]([Br:24])[cH:21][cH:22][cH:23]2)[c:9]2[cH:10][cH:11][cH:12][cH:13][c:14]2[c:15]1=[O:16])[CH3:25].[CH:27]([CH3:28])([CH3:29])[c:30]1[cH:31][cH:32][c:33]([Mg+:36])[cH:34][cH:35]1>>[C:4](=[O:5])([c:6]1[cH:7][n:8]([CH2:17][c:18]2[n:19][c:20]([Br:24])[cH:21][cH:22][cH:23]2)[c:9]2[cH:10][cH:11][cH:12][cH:13][c:14]2[c:15]1=[O:16])[c:33]1[cH:32][cH:31][c:30]([CH:27]([CH3:28])[CH3:29])[cH:35][cH:34]1

Participants

5

Reactant 4

HCID 259Bromide ionHCID 8028TetrahydrofuranHCID 577545321-(6-Bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amideHCID 178439195HCID 178439195, compound

Product 1

HCID 577545951-(6-Bromo-pyridin-2-ylmethyl)-3-(4-isopropyl-benzoyl)-1H-quinolin-4-one

Sources & evidence

ORD record
ord-df3036ce8ef04ec18d338e4f07504da9
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (6/10)

Reaction notes

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