HCID 15949507, compound → HCID 57666161, compound
Reaction equation
[CH:1]1([C:4]2[N:5]=[CH:6][C:7]3[CH2:12][N:11]([C@@H:13]4[CH2:18][C@H:17]([NH2:19])[C@@H:16]([C:20]5[CH:25]=[C:24]([F:26])[C:23]([F:27])=[CH:22][C:21]=5[F:28])[CH2:15][CH2:14]4)[CH2:10][C:8]=3[N:9]=2)[CH2:3][CH2:2]1.O=C1C[C@H](NC(=O)OCC2C=CC=CC=2)[C@@H](C2C=C(F)C(F)=CC=2F)CC1>CO.[Pd]>[CH:1]1([C:4]2[N:5]=[CH:6][C:7]3[C:8](=[CH:10][N:11]([C@@H:13]4[CH2:18][C@H:17]([NH2:19])[C@@H:16]([C:20]5[CH:25]=[C:24]([F:26])[C:23]([F:27])=[CH:22][C:21]=5[F:28])[CH2:15][CH2:14]4)[CH:12]=3)[N:9]=2)[CH2:2][CH2:3]1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of [(1S,2R,5S)-5-[2-cyclopropyl-5,7-dihydro-6H-pyrrolo[3,4-d]pyrimidin-6-yl]-2-(2,4,5-trifluorophenyl)cyclohexyl]amine described in Example 2 (30.0 mg) in methanol (6 mL) was stirred with 10% palladium on carbon (6 mg) for seven days and the resulting product was purified by preparative TLC (silica, 7:93 methanol/dichloromethane) to give the title compound. LC-MS 387.3 (M+1).
Workup
- customthe resulting product was purified by preparative TLC (silica, 7:93 methanol/dichloromethane)
Sources & evidence
- ORD record
- ord-cc6b6c7e027c410488572c49e491642b
- Source dataset
- uspto-grants-2011_03
- Patent number
- US07906649B2
Reaction notes
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