HCID 59021554, compound → HCID 59021465, compound
Reaction equation
[C:1]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]2[C:13]3[CH2:28][CH2:27][N:26](CC4C=CC=CC=4)[CH2:25][C:14]=3[N:15]=[C:16]([CH2:18][N:19]3[CH2:24][CH2:23][O:22][CH2:21][CH2:20]3)[N:17]=2)=[CH:7][CH:6]=1)([CH3:4])([CH3:3])[CH3:2]>CO.[OH-].[OH-].[Pd+2]>[C:1]([C:5]1[CH:10]=[CH:9][C:8]([NH:11][C:12]2[C:13]3[CH2:28][CH2:27][NH:26][CH2:25][C:14]=3[N:15]=[C:16]([CH2:18][N:19]3[CH2:20][CH2:21][O:22][CH2:23][CH2:24]3)[N:17]=2)=[CH:7][CH:6]=1)([CH3:4])([CH3:2])[CH3:3]Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A catalytic amount palladium hydroxide on carbon powder (20% Pd moisture ea. 60%) was added to a solution of N-(4-tert-butylphenyl)-7-benzyl-5,6,7,8-tetrahydro-2-(morpholinomethyl)pyrido[3,4-d]pyrimidin-4-amine (240 mg, 0.51 mmol) in methanol and was stirred under a hydrogen filled balloon over night at room temperature. Reaction solution was filtered through celite and filtrate was concentrated to yield the product as a white powder (150 mg).
Workup
- customReaction solution
- filtrationwas filtered through celite and filtrate
- concentrationwas concentrated
Sources & evidence
- ORD record
- ord-b6758ac16eea47c8b90092ec63013a6a
- Source dataset
- uspto-grants-2007_12
- Patent number
- US07312330B2
Reaction notes
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