Dimethylformamide → HCID 58043132, compound

HRID 701328Notes

Reaction equation

HRID 701328 reaction equation
[C:28](=[O:29])([O-:30])[O-:31].[CH3:12][S:13]([O:14][CH:17]1[CH2:18][N:19]([C:21](=[O:22])[O:23][C:24]([CH3:25])([CH3:26])[CH3:27])[CH2:20]1)(=[O:15])=[O:16].[CH3:34][CH2:35][O:36][C:37]([CH3:38])=[O:39].[Cs+:32].[Cs+:33].[O:40]=[CH:41][N:42]([CH3:43])[CH3:44].[SH:1][c:2]1[cH:3][cH:4][c:5]([C:6](=[O:7])[O:8][CH3:9])[cH:10][cH:11]1>>[S:1]([c:2]1[cH:3][cH:4][c:5]([C:6](=[O:7])[O:8][CH3:9])[cH:10][cH:11]1)[CH:17]1[CH2:18][N:19]([C:21](=[O:22])[O:23][C:24]([CH3:25])([CH3:26])[CH3:27])[CH2:20]1

Participants

7

Reactant 6

HCID 6228DimethylformamideHCID 8857Ethyl AcetateHCID 19660Carbonate IonHCID 104967Cesium cation2×HCID 237573Methyl 4-sulfanylbenzoateHCID 10753243Tert-butyl 3-(methanesulfonyloxy)azetidine-1-carboxylate

Product 1

HCID 58043132HCID 58043132, compound

Sources & evidence

ORD record
ord-335e32adbc2f40218f49b9ab35bd96b7
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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