Cyclobutanesulfonamide → HCID 178438871, compound

HRID 121367Notes

Reaction equation

HRID 121367 reaction equation
[CH2:1]([CH:2]=[CH2:3])[C:4]1([CH3:30])[C:5](=[O:29])[N:6]([CH:24]([CH2:25][OH:26])[CH2:27][CH3:28])[CH:7]([c:17]2[cH:18][cH:19][c:20]([Cl:23])[cH:21][cH:22]2)[CH:8]([c:10]2[cH:11][c:12]([Cl:16])[cH:13][cH:14][cH:15]2)[CH2:9]1.[CH:31]1([S:35](=[O:36])(=[O:37])[NH2:38])[CH2:32][CH2:33][CH2:34]1>>[CH2:1]([CH:2]=[CH2:3])[C:4]1([CH3:30])[C:5](=[O:29])[N:6]([CH:24]([CH2:25][NH:38][S:35]([CH:31]2[CH2:32][CH2:33][CH2:34]2)(=[O:36])=[O:37])[CH2:27][CH3:28])[CH:7]([c:17]2[cH:18][cH:19][c:20]([Cl:23])[cH:21][cH:22]2)[CH:8]([c:10]2[cH:11][c:12]([Cl:16])[cH:13][cH:14][cH:15]2)[CH2:9]1

Participants

3

Reactant 2

HCID 15238957CyclobutanesulfonamideHCID 768344715-(3-Chlorophenyl)-6-(4-chlorophenyl)-1-(1-hydroxybutan-2-yl)-3-methyl-3-prop-2-enylpiperidin-2-one

Product 1

HCID 178438871HCID 178438871, compound

Sources & evidence

ORD record
ord-823c234fc14747709c3a4e74efe6fc8f
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (2/10)

Reaction notes

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