p-(Methylsulphonyl)benzoic acid → HCID 178465967, compound

HRID 347990Notes

Reaction equation

HRID 347990 reaction equation
[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[CH2:6][C:5]1=[O:16])(=[O:3])[CH3:2].[CH3:17][S:18]([C:21]1[CH:29]=[CH:28][C:24]([C:25](O)=[O:26])=[CH:23][CH:22]=1)(=[O:20])=[O:19]>>[C:1]([N:4]1[C:12]2[C:7](=[CH:8][C:9]([C:13](=[O:15])[CH3:14])=[CH:10][CH:11]=2)[C:6](=[C:25]([C:24]2[CH:23]=[CH:22][C:21]([S:18]([CH3:17])(=[O:20])=[O:19])=[CH:29][CH:28]=2)[OH:26])[C:5]1=[O:16])(=[O:3])[CH3:2]

Participants

3

Reactant 2

HCID 77670p-(Methylsulphonyl)benzoic acidHCID 210845601,5-Diacetyl-2-indolinone

Product 1

HCID 178465967HCID 178465967, compound

Procedure

Prepared from 1,5-diacetyl-2-indolinone and 4-methylsulphonyl-benzoic acid

Sources & evidence

ORD record
ord-a729a0dd161e4ae3b83d906da56f0a4c
Source dataset
uspto-grants-2007_02
Patent number
US07176231B2

Reaction notes

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