Chloride → HCID 57754709, compound

HRID 1132357Notes

Reaction equation

HRID 1132357 reaction equation
[CH2:41]1[O:42][CH2:43][CH2:44][CH2:45]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:37]([Mg+:38])([CH3:39])[CH3:40].[Cl-:36].[I:26][c:27]1[cH:28][cH:29][c:30]([O:34][CH3:35])[c:31]([CH3:33])[n: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][cH:29][c:30]([O:34][CH3:35])[c:31]([CH3:33])[n: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 58866081HCID 58866081, compoundHCID 178461726HCID 178461726, compound

Product 1

HCID 57754709HCID 57754709, compound

Sources & evidence

ORD record
ord-83578199682b4d4b8523f88c95b98300
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (7/10)

Reaction notes

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