Diethylamine → HCID 66914259, compound
Reaction equation
Cl[CH2:2][C:3]1[CH:38]=[CH:37][C:6]([CH2:7][O:8][C:9]2[CH:10]=[C:11]([C:15]3[C:24]4[C:19](=[C:20]([C:25]([F:28])([F:27])[F:26])[CH:21]=[CH:22][CH:23]=4)[N:18]=[CH:17][C:16]=3[C:29]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=3)=[O:30])[CH:12]=[CH:13][CH:14]=2)=[CH:5][CH:4]=1.[CH2:39]([NH:41][CH2:42][CH3:43])[CH3:40]>C(Cl)Cl>[CH2:39]([N:41]([CH2:2][C:3]1[CH:38]=[CH:37][C:6]([CH2:7][O:8][C:9]2[CH:10]=[C:11]([C:15]3[C:24]4[C:19](=[C:20]([C:25]([F:28])([F:27])[F:26])[CH:21]=[CH:22][CH:23]=4)[N:18]=[CH:17][C:16]=3[C:29]([C:31]3[CH:36]=[CH:35][CH:34]=[CH:33][CH:32]=3)=[O:30])[CH:12]=[CH:13][CH:14]=2)=[CH:5][CH:4]=1)[CH2:42][CH3:43])[CH3:40]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of {4-[3-(4-chloromethyl-benzyloxy)-phenyl]-8-trifluoromethyl-quinolin-3-yl}phenyl-methanone (011 g, 0.2 mmol) and diethylamine(0.3 g, 5.7 mmol) in CH2Cl2 (5 ml) was stirred at r.t. After 24 hr, the reaction was concentrated and purified by column chromatography (eluent 25% EtOAc/Hex) to give the title compound as a foam (0.10 g); MS m/z 569.
Workup
- concentrationthe reaction was concentrated
- custompurified by column chromatography (eluent 25% EtOAc/Hex)
Sources & evidence
- ORD record
- ord-7c1290aeece4486bb88a06a25325854c
- Source dataset
- uspto-grants-2009_08
- Patent number
- US07576215B2
Reaction notes
Loading…