2-(2,2,2-Trifluoroethoxy)ethan-1-ol → 1-(t-butoxycarbonyl)-4-(1-(2-(2,2,2-trifluoroethoxy)ethyl)-1H-benzimidazole-2-carbonyl)piperidine
Reaction equation
[F:1][C:2]([F:9])([F:8])[CH2:3][O:4][CH2:5][CH2:6]O.[C:10]([O:14][C:15]([N:17]1[CH2:22][CH2:21][CH:20]([C:23]([C:25]2[NH:29][C:28]3[CH:30]=[CH:31][CH:32]=[CH:33][C:27]=3[N:26]=2)=[O:24])[CH2:19][CH2:18]1)=[O:16])([CH3:13])([CH3:12])[CH3:11]>>[C:10]([O:14][C:15]([N:17]1[CH2:18][CH2:19][CH:20]([C:23]([C:25]2[N:26]([CH2:6][CH2:5][O:4][CH2:3][C:2]([F:1])([F:8])[F:9])[C:27]3[CH:33]=[CH:32][CH:31]=[CH:30][C:28]=3[N:29]=2)=[O:24])[CH2:21][CH2:22]1)=[O:16])([CH3:13])([CH3:11])[CH3:12]Participants
3
Procedure
Prepare by the method of Preparation 9 using 2-hydroxyethyl 2,2,2-trifluorethyl ether and 1-(t-butoxycarbonyl)-4-(1H-benzimidazole-2-carbonyl)piperidine (2.0 g, 6.1 mmol) to give 1-(t-butoxycarbonyl)-4-(1-(2-(2,2,2-trifluoroethoxy)ethyl)-1H-benzimidazole-2-carbonyl)piperidine.
Sources & evidence
- ORD record
- ord-4f085489e0814f99bcca32c4895b31db
- Source dataset
- uspto-grants-2001_10
- Patent number
- US06297259B1
Reaction notes
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