Potassium Cation → 3-(2-Oxopyrrolidin-1-yl)-4-phenoxy-5-sulfamoylbenzoic acid

HRID 688275Notes

Reaction equation

HRID 688275 reaction equation
[C:28](=[O:29])([O-:30])[O-:31].[Cl:1][CH2:2][CH2:3][CH2:4][C:5](=[O:6])[NH:7][c:8]1[cH:9][c:10]([C:11](=[O:12])[OH:13])[cH:14][c:15]([S:24]([NH2:25])(=[O:26])=[O:27])[c:16]1[O:17][c:18]1[cH:19][cH:20][cH:21][cH:22][cH:23]1.[K+:32].[K+:33].[O:34]1[CH2:35][CH2:36][O:37][CH2:38][CH2:39]1>>[CH2:2]1[CH2:3][CH2:4][C:5](=[O:6])[N:7]1[c:8]1[cH:9][c:10]([C:11](=[O:12])[OH:13])[cH:14][c:15]([S:24]([NH2:25])(=[O:26])=[O:27])[c:16]1[O:17][c:18]1[cH:19][cH:20][cH:21][cH:22][cH:23]1

Participants

5

Reactant 4

HCID 813Potassium Cation2×HCID 19660Carbonate IonHCID 312751,4-DioxaneHCID 3219633-(4-chlorobutanoylamino)-4-phenoxy-5-sulfamoylbenzoic acid

Product 1

HCID 203345293-(2-Oxopyrrolidin-1-yl)-4-phenoxy-5-sulfamoylbenzoic acid

Sources & evidence

ORD record
ord-d71e2e88d0964290a293e24e92f2a378
Source dataset
Training data from https://doi.org/10.1039/C8SC04228D (3/10)

Reaction notes

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