Dimethyl Sulfoxide → HCID 178422193, compound

HRID 115404Notes

Reaction equation

[C:11]([CH3:12])([CH3:13])([CH3:14])[O:15][C:16](=[O:17])[N:18]1[CH:19]([CH2:27][OH:28])[CH:20]2[CH2:21][CH:22]([CH3:26])[CH2:23][CH:24]2[CH2:25]1.[CH3:7][S:8]([CH3:9])=[O:10].[CH:29]([N:30]([CH2:31][CH3:32])[CH:33]([CH3:34])[CH3:35])([CH3:36])[CH3:37].[Cl:1][C:2]([C:3]([Cl:4])=[O:5])=[O:6].[Cl:38][CH2:39][Cl:40].[OH2:41]>>[C:11]([CH3:12])([CH3:13])([CH3:14])[O:15][C:16](=[O:17])[N:18]1[CH:19]([CH:27]=[O:28])[CH:20]2[CH2:21][CH:22]([CH3:26])[CH2:23][CH:24]2[CH2:25]1

Participants

Reactant 6

HCID 679Dimethyl Sulfoxide

HCID 962Water

HCID 6344Dichloromethane

HCID 65578Oxalyl chloride

HCID 81531Diisopropylethylamine

HCID 178422194tert-butyl 3-(hydroxymethyl)-5-methyl-3,3a,4,5,6,6a-hexahydro-1H-cyclopenta[c]pyrrole-2-carboxylate

Product 1

HCID 178422193HCID 178422193, compound

Sources & evidence

ORD record: ord-80bf4def421a4f8ca0e2eba9e5735f02
Source dataset: Training data from https://doi.org/10.1039/C8SC04228D (2/10)
DOI: 10.1039/C8SC04228D

Reaction notes

Loading…