Chloride → HCID 57754755, compound

HRID 2159978Notes

Reaction equation

HRID 2159978 reaction equation
[CH2:26]([CH3:27])[O:28][c:29]1[c:30]([CH3:36])[cH:31][c:32]([I:35])[cH:33][cH:34]1.[CH2:42]1[O:43][CH2:44][CH2:45][CH2:46]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:38]([Mg+:39])([CH3:40])[CH3:41].[Cl-:37]>>[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:32]1[cH:31][c:30]([CH3:36])[c:29]([O:28][CH2:26][CH3:27])[cH:34][cH:33]1

Participants

6

Reactant 5

HCID 312ChlorideHCID 8028TetrahydrofuranHCID 21999882HCID 21999882, compoundHCID 577545321-(6-Bromo-pyridin-2-ylmethyl)-4-oxo-1,4-dihydro-quinoline-3-carboxylic acid methoxy-methyl-amideHCID 178461726HCID 178461726, compound

Product 1

HCID 57754755HCID 57754755, compound

Sources & evidence

ORD record
ord-db1c682631354bae9136ec9bc6aa91e4
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (4/10)

Reaction notes

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