Aniline → HCID 178503386, compound
Reaction equation
F[C:2]1[CH:7]=[C:6]([C:8]2[NH:9][C:10]([S:20][CH3:21])=[N:11][C:12]=2[C:13]2[CH:18]=[CH:17][C:16]([F:19])=[CH:15][CH:14]=2)[CH:5]=[CH:4][N:3]=1.[NH2:22][C:23]1[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=1>>[F:19][C:16]1[CH:17]=[CH:18][C:13]([C:12]2[N:11]=[C:10]([S:20][CH3:21])[NH:9][C:8]=2[C:6]2[CH:5]=[CH:4][N:3]=[C:2]([NH:22][C:23]3[CH:28]=[CH:27][CH:26]=[CH:25][CH:24]=3)[CH:7]=2)=[CH:14][CH:15]=1Participants
3
Procedure
Using the general method C, the title compound was prepared from 25b (0.2 g; 0.7 mmol) and aniline (0.65 g; 7.0 mmol) after a reaction time of 6 hours under reflux and separation by column chromatography (SiO2 60, CH2Cl2/EtOH 9+1). M.p. 228° C.
Workup
- temperatureunder reflux
- customseparation by column chromatography (SiO2 60, CH2Cl2/EtOH 9+1)
Sources & evidence
- ORD record
- ord-5d1c9f2c839c4f6d8bcacb0790b12a7e
- Source dataset
- uspto-grants-2009_09
- Patent number
- US07582660B2
Reaction notes
Loading…