Bromide ion → 1-(6-Bromo-pyridin-2-ylmethyl)-3-(5-chloro-thiophene-2-carbonyl)-1H-quinolin-4-one

HRID 166474Notes

Reaction equation

HRID 166474 reaction equation
[Br-:26].[CH2:34]1[O:35][CH2:36][CH2:37][CH2:38]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].[Cl:27][c:28]1[cH:29][cH:30][c:31]([Mg+:33])[s:32]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:31]1[cH:30][cH:29][c:28]([Cl:27])[s:32]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 178507013HCID 178507013, compound

Product 1

HCID 577547331-(6-Bromo-pyridin-2-ylmethyl)-3-(5-chloro-thiophene-2-carbonyl)-1H-quinolin-4-one

Sources & evidence

ORD record
ord-205a152fe4f5426ab8a2a83a28a7e71c
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (9/10)

Reaction notes

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