Bromide ion → HCID 57754686, compound

HRID 1221350Notes

Reaction equation

HRID 1221350 reaction equation
[Br-:26].[CH2:36]1[O:37][CH2:38][CH2:39][CH2:40]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].[CH3:27][c:28]1[c:29]([Mg+:35])[cH:30][c:31]([CH3:34])[cH:32][cH:33]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:29]1[c:28]([CH3:27])[cH:33][cH:32][c:31]([CH3:34])[cH:30]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 178425075HCID 178425075, compound

Product 1

HCID 57754686HCID 57754686, compound

Sources & evidence

ORD record
ord-b600f824de6f4095b56e7f01aa884a18
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)

Reaction notes

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