HCID 71208212, compound → HCID 71217347, compound

HRID 689348Notes

Reaction equation

HRID 689348 reaction equation
[Cl:21][c:22]1[cH:23][c:24]([CH2:25][n:26]2[c:27](=[O:35])[cH:28][c:29]([C:32](=[O:33])[OH:34])[cH:30][cH:31]2)[cH:36][cH:37][cH:38]1.[NH2:1][CH2:2][c:3]1[cH:4][n:5](-[c:15]2[cH:16][cH:17][cH:18][cH:19][cH:20]2)[c:6]2[cH:7][c:8]([Cl:14])[cH:9][cH:10][c:11]2[c:12]1=[O:13]>>[NH:1]([CH2:2][c:3]1[cH:4][n:5](-[c:15]2[cH:16][cH:17][cH:18][cH:19][cH:20]2)[c:6]2[cH:7][c:8]([Cl:14])[cH:9][cH:10][c:11]2[c:12]1=[O:13])[C:32]([c:29]1[cH:28][c:27](=[O:35])[n:26]([CH2:25][c:24]2[cH:23][c:22]([Cl:21])[cH:38][cH:37][cH:36]2)[cH:31][cH:30]1)=[O:33]

Participants

3

Reactant 2

HCID 71208212HCID 71208212, compoundHCID 712083983-(aminomethyl)-7-chloro-1-phenylquinolin-4(1H)-one

Product 1

HCID 71217347HCID 71217347, compound

Sources & evidence

ORD record
ord-878c8fdd5a43414c967aa4cfb8d462fd
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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