7-[(R)-1-(2,6-Dichloro-3-fluorophenyl)ethoxy]-3-(1,2,3,6-tetrahydropyridin-4-yl)furo[3,2-c]pyridin-6-ylamine → 7-[(R)-1-(2,6-Dichloro-3-fluorophenyl)-ethoxy]-3-piperidin-4-yl-furo[3,2-c]pyridin-6-ylamine
Reaction equation
[Cl:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[C:4]([Cl:9])[C:3]=1[C@H:10]([O:12][C:13]1[C:14]2[O:22][CH:21]=[C:20]([C:23]3[CH2:24][CH2:25][NH:26][CH2:27][CH:28]=3)[C:15]=2[CH:16]=[N:17][C:18]=1[NH2:19])[CH3:11]>CCOC(C)=O.[Pd]>[Cl:1][C:2]1[C:7]([F:8])=[CH:6][CH:5]=[C:4]([Cl:9])[C:3]=1[C@H:10]([O:12][C:13]1[C:14]2[O:22][CH:21]=[C:20]([CH:23]3[CH2:24][CH2:25][NH:26][CH2:27][CH2:28]3)[C:15]=2[CH:16]=[N:17][C:18]=1[NH2:19])[CH3:11]Participants
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 7-[(R)-1-(2,6-dichloro-3-fluorophenyl)-ethoxy]-3-(1,2,3,6-tetrahydropyridin-4-yl)-furo[3,2-c]pyridin-6-ylamine (5.00 mg, 0.0118 mmol) in EtOAc (2 mL) with palladium (0.53 mg, 0.0050 mmol) on carbon was sealed and flushed with a nitrogen balloon at rt. The nitrogen balloon was replaced with a hydrogen balloon, and the mixture was allowed to stir for 1 h. The hydrogen balloon was removed and replaced with the nitrogen balloon to flush out all hydrogen gas. The palladium was filtered off, and the product was loaded onto a preparatory TLC plate, eluting with 10% (7 N NH3 in MeOH) in DCM to afford the title compound as a yellow solid. 1H NMR (CD3OD, 400 MHz): δ=1.62 (br, s, 2H), 1.83 (d, J=6.8 Hz, 3H), 2.09-2.22 (m, 2H), 2.70-2.85 (m, 3H), 3.11 (br, s, 2H), 6.50-6.57 (m, 1H), 7.10 (t, J=8.5 Hz, 1H), 7.24 (s, 1H), 7.31 (dd, J=9.1, 4.8 Hz, 1H), 7.95 (s, 1H).
Workup
- customflushed with a nitrogen balloon at rt
- customThe hydrogen balloon was removed
- customto flush out all hydrogen gas
- filtrationThe palladium was filtered off
- washeluting with 10% (7 N NH3 in MeOH) in DCM
Sources & evidence
- ORD record
- ord-a22fd0dfa36f42eba0f4833f856bbff9
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08022206B2
Reaction notes
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