2,4-Difluoroaniline → HCID 15295063, compound
Reaction equation
[CH2:1]([N:13]1[N:17]=[N:16][C:15]([CH2:18][CH2:19][C:20]([OH:22])=O)=[N:14]1)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].[F:23][C:24]1[CH:30]=[C:29]([F:31])[CH:28]=[CH:27][C:25]=1[NH2:26]>>[F:23][C:24]1[CH:30]=[C:29]([F:31])[CH:28]=[CH:27][C:25]=1[NH:26][C:20](=[O:22])[CH2:19][CH2:18][C:15]1[N:16]=[N:17][N:13]([CH2:1][CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12])[N:14]=1Participants
3
Procedure
In a manner similar to Example 34, 2-dodecyl-2H-tetrazole-5-propanoic acid was condensed with 2,4-difluoroaniline to give the title compound, mp 86°-87° C.
Sources & evidence
- ORD record
- ord-37c0c1ad57d249eda9cd65c7b6d88af4
- Source dataset
- uspto-grants-1995_08
- Patent number
- US05441975
Reaction notes
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