2,2-Difluoro-1,3-benzodioxole-5-carboxylic acid → HCID 178465954, compound
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].[F:17][C:18]1([F:30])[O:22][C:21]2[CH:23]=[CH:24][C:25]([C:27](O)=[O:28])=[CH:26][C:20]=2[O:19]1>>[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:27]([C:25]2[CH:24]=[CH:23][C:21]3[O:22][C:18]([F:30])([F:17])[O:19][C:20]=3[CH:26]=2)[OH:28])[C:5]1=[O:16])(=[O:3])[CH3:2]Participants
3
Procedure
Prepared from 1,5-diacetyl-2-indolinone and 2,2-difluoro-benzo[1,3]dioxol-5-carboxylic acid
Sources & evidence
- ORD record
- ord-bbe8e2a512124782894d8c4529b4bec3
- Source dataset
- uspto-grants-2009_07
- Patent number
- US07560480B2
Reaction notes
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