2-Methylimidazoline → HCID 59553146, compound

HRID 1231328Notes

Reaction equation

HRID 1231328 reaction equation
[CH3:38][C:39]1=[N:43][CH2:42][CH2:41][NH:40]1.[F:1][c:2]1[cH:3][c:4]([C:5](=[O:6])[NH:7][c:8]2[cH:9][cH:10][c:11]([O:18][c:19]3[n:20][c:21]([S:25]([CH3:26])(=[O:27])=[O:28])[n:22][cH:23][cH:24]3)[c:12]3[cH:13][cH:14][cH:15][cH:16][c:17]23)[cH:29][c:30]([N:32]2[CH2:33][CH2:34][CH2:35][CH2:36][CH2:37]2)[cH:31]1>>[F:1][c:2]1[cH:3][c:4]([C:5](=[O:6])[NH:7][c:8]2[cH:9][cH:10][c:11]([O:18][c:19]3[n:20][c:21]([N:43]4[C:39]([CH3:38])=[N:40][CH2:41][CH2:42]4)[n:22][cH:23][cH:24]3)[c:12]3[cH:13][cH:14][cH:15][cH:16][c:17]23)[cH:29][c:30]([N:32]2[CH2:33][CH2:34][CH2:35][CH2:36][CH2:37]2)[cH:31]1

Participants

3

Reactant 2

HCID 107982-MethylimidazolineHCID 667379693-fluoro-N-[4-(2-methanesulfonyl-pyrimidin-4-yloxy)-naphthalen-1-yl]-5-piperidin-1-yl-benzamide

Product 1

HCID 59553146HCID 59553146, compound

Sources & evidence

ORD record
ord-0c641516d4b14632a3ec07ab7c32f13a
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (5/10)

Reaction notes

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