Chloride → HCID 57754741, compound

HRID 300281Notes

Reaction equation

HRID 300281 reaction equation
[CH2:44]1[O:45][CH2:46][CH2:47][CH2:48]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:40]([Mg+:41])([CH3:42])[CH3:43].[Cl-:39].[I:26][c:27]1[cH:28][c:29]([CH3:38])[c:30]([O:33][CH2:34][CH2:35][O:36][CH3:37])[cH:31][cH: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:27]1[cH:28][c:29]([CH3:38])[c:30]([O:33][CH2:34][CH2:35][O:36][CH3:37])[cH:31][cH:32]1

Participants

6

Reactant 5

HCID 312ChlorideHCID 8028TetrahydrofuranHCID 577545321-(6-Bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amideHCID 66879118HCID 66879118, compoundHCID 178461726HCID 178461726, compound

Product 1

HCID 57754741HCID 57754741, compound

Sources & evidence

ORD record
ord-66dbb7d60c524ed6ac4e258a8e5e5411
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (8/10)

Reaction notes

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