HCID 11844929, compound → HCID 11844928, compound
Reaction equation
[CH:1]1([CH2:7][NH:8][C:9]([C:11]2[C:12]3[CH2:20][CH2:19][N:18](CC4C=CC=CC=4)[CH2:17][C:13]=3[N:14]=[CH:15][N:16]=2)=[O:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1>[Pd]>[CH:1]1([CH2:7][NH:8][C:9]([C:11]2[C:12]3[CH2:20][CH2:19][NH:18][CH2:17][C:13]=3[N:14]=[CH:15][N:16]=2)=[O:10])[CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1Participants
3
Reactant 1
Product 1
Reagents, catalysts & solvents 1
Procedure
Into a 500 ml hydrogenation vessel was combined 7-benzyl-5,6,7,8-tetrahydropyrido[3,4-d]pyrimidine-4-carboxylic acid, cyclohexylmethyl-amide (80 mg, 0.22 mmol), palladium on carbon (30 mg) and methano. The vessel was purged and evacuated with hydrogen three times and allowed to agitate overnight at 15 psi. The contents were filtered over celite and concentrated to afford the title compound (4.7 mg, 7.7%.
Workup
- customInto a 500 ml hydrogenation vessel was combined
- customThe vessel was purged
- customevacuated with hydrogen three times
- filtrationThe contents were filtered over celite and
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-be3167e02d4b43e88492a5f69cdbc54e
- Source dataset
- uspto-grants-2014_07
- Patent number
- US08779144B2
Reaction notes
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