Reaction equation
[ClH:1].[N:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][CH:4]([C@@H:5]3[NH2:12])[CH2:3]1)[CH2:9]2.[F:13][C:14]([F:30])([F:29])[C:15]1[CH:16]=[C:17]([C:21]2[O:25][C:24]([C:26](O)=[O:27])=[CH:23][CH:22]=2)[CH:18]=[CH:19][CH:20]=1.N>>[ClH:1].[N:2]12[CH2:11][CH:6]3[CH2:7][CH:8]([CH2:10][CH:4]([C@@H:5]3[NH:12][C:26]([C:24]3[O:25][C:21]([C:17]4[CH:18]=[CH:19][CH:20]=[C:15]([C:14]([F:30])([F:13])[F:29])[CH:16]=4)=[CH:22][CH:23]=3)=[O:27])[CH2:3]1)[CH2:9]2Participants
4
Procedure
Prepared from (4s)-1-azatricyclo[3.3.1.13,7]dec-4-ylamine hydrochloride and 5-[3-(trifluoromethyl)phenyl]-2-furoic acid (Aldrich) according to methods A and C; yield 44 mg, 0.11 mmol (51%): 1H NMR (300 MHz, methanol-d4) δ 1.99 (d, J=14 Hz, 2H), 2.22 (s, 1H), 2.34 (d, J=14 Hz, 2H), 2.52 (s, 2H), 3.58 (s, 2H), 3.69 (s, 4H), 4.43 (s, 1H), 7.12 (d, J=4 Hz, 1H), 7.34 (d, J=4 Hz, 1H), 7.64-7.69 (m, 2H), 8.11-8.17 (m, 1H), 8.24 (s, 1H); MS (DCI/NH3) m/z 391 (M+H)+; Anal. C21H21F3N2O2.HCl: C, H, N.
Sources & evidence
- ORD record
- ord-6c0c400b061e4b5db41b728b6ff1417d
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07897766B2
Linked notes
Loading…