4-[(Diethylamino)methyl]benzoic acid → HCID 178463924, 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].[CH2:17]([N:19]([CH2:22][C:23]1[CH:31]=[CH:30][C:26]([C:27](O)=[O:28])=[CH:25][CH:24]=1)[CH2:20][CH3:21])[CH3:18]>>[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:26]2[CH:30]=[CH:31][C:23]([CH2:22][N:19]([CH2:20][CH3:21])[CH2:17][CH3:18])=[CH:24][CH:25]=2)[OH:28])[C:5]1=[O:16])(=[O:3])[CH3:2]Participants
3
Procedure
Prepared from 1,5-diacetyl-2-indolinone and 4-diethylaminomethyl-benzoic acid
Sources & evidence
- ORD record
- ord-24ca75d8bf154c7387a98c9e624d4259
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07176231B2
Reaction notes
Loading…