Butylamine → HCID 86612517, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([CH2:9][CH:10]([NH:18][C:19]([C:21]2[C:27]3[CH:28]=[CH:29][CH:30]=[CH:31][C:26]=3[O:25][C:24]3[CH:32]=[CH:33][CH:34]=[CH:35][C:23]=3[CH:22]=2)=[O:20])[CH:11]2[CH2:15][CH:14]([CH3:16])[C:13](=[O:17])[O:12]2)[CH:5]=[C:6]([F:8])[CH:7]=1.[CH2:36]([NH2:40])[CH2:37][CH2:38][CH3:39]>>[CH2:36]([NH:40][C:13]([CH:14]([CH3:16])[CH2:15][CH:11]([OH:12])[CH:10]([NH:18][C:19]([C:21]1[C:27]2[CH:28]=[CH:29][CH:30]=[CH:31][C:26]=2[O:25][C:24]2[CH:32]=[CH:33][CH:34]=[CH:35][C:23]=2[CH:22]=1)=[O:20])[CH2:9][C:4]1[CH:5]=[C:6]([F:8])[CH:7]=[C:2]([F:1])[CH:3]=1)=[O:17])[CH2:37][CH2:38][CH3:39]Participants
3
Procedure
Dibenzo[b,f]oxepine-10-carboxylic acid [2-(3,5-difluoro-phenyl)-1-(4-methyl-5-oxo-tetrahydrofuran-2-yl)-ethyl]-amide (50 mg, 0.105 mmol) is dissolved in 2 ml butylamine and stirred for 16 h. The solution is concentrated in vacuo and the residual solid recrystallized from EtOAc/hexane. Yield 27 mg (48%).
Workup
- concentrationThe solution is concentrated in vacuo
- customthe residual solid recrystallized from EtOAc/hexane
Sources & evidence
- ORD record
- ord-57283b9ee7444990b5620da211b5dd22
- Source dataset
- uspto-grants-2009_11
- Patent number
- US07612054B2
Reaction notes
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