2,4-Difluoroaniline → HCID 15230638, compound
Reaction equation
[CH2:1]([N:13]1[N:17]=[N:16][C:15]([NH:18][C:19]2[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=2)=[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].ClC(Cl)(O[C:29](=[O:35])OC(Cl)(Cl)Cl)Cl.[F:37][C:38]1[CH:44]=[C:43]([F:45])[CH:42]=[CH:41][C:39]=1[NH2:40]>>[F:37][C:38]1[CH:44]=[C:43]([F:45])[CH:42]=[CH:41][C:39]=1[NH:40][C:29](=[O:35])[N: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]=1)[C:19]1[CH:24]=[CH:23][CH:22]=[CH:21][CH:20]=1Participants
4
Procedure
In a manner similar to Example 1, 2-dodecyl-N-phenyl-2H-tetrazol-5-amine was reacted with triphosgene and 2,4-difluoroaniline to give the title compound, mp=55°-57° C.
Sources & evidence
- ORD record
- ord-354312747b784f4ebb4521363d11b9cb
- Source dataset
- uspto-grants-1994_11
- Patent number
- US05362744
Reaction notes
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