Ethanol → HCID 20027830, compound
Reaction equation
[CH3:1][C:2]12[CH2:8][C:6]([C:9]3[CH:14]=[CH:13][C:12]([N+:15]([O-])=O)=[CH:11][CH:10]=3)([CH2:7]1)[C:5](=[O:18])[NH:4][C:3]2=[O:19].C(O)C>COCCO.[Pd]>[NH2:15][C:12]1[CH:11]=[CH:10][C:9]([C:6]23[CH2:8][C:2]([CH3:1])([CH2:7]2)[C:3](=[O:19])[NH:4][C:5]3=[O:18])=[CH:14][CH:13]=1Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
In a manner analogous to that described in Example 12a, 3.7 g of 5-methyl-1-(4-nitrophenyl)-3-azabicyclo[3.1.1]heptane-2,4-dione in 80 ml of 2-methoxyethanol are hydrogenated in the presence of 0.4 g of 5% palladium-on-carbon and worked up. Melting point 216° (from ethanol).
Sources & evidence
- ORD record
- ord-f50d021703884aa587913d6857e3085a
- Source dataset
- uspto-grants-1987_06
- Patent number
- US04677129
Reaction notes
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