HCID 20378662, compound → HCID 20378672, compound
Reaction equation
[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]1[CH2:12][CH2:13][N:14](C(OCC3C=CC=CC=3)=O)[CH2:15][CH:7]1[C:6](=[O:26])[NH:5]2>[Pd].C(O)C>[NH2:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]1[CH2:12][CH2:13][NH:14][CH2:15][CH:7]1[C:6](=[O:26])[NH:5]2Participants
4
Reactant 1
Product 1
Reagents, catalysts & solvents 2
Procedure
A mixture of 1.5 g. of 8amino-3-carbobenzoxy-2,3,4,4a-tetrahydro-1H-pyrazino[1,2-a]quinoxalin-5-(6H)-one, 1.5 g. of 10% Palladium on carbon catalyst and 150 ml. of ethanol is hydrogenated for 1/2 hour at 45 p.s.i. The catalyst is filtered and the filtrate concentrated to a volume of 50 ml. Ethanolic hydrochloric acid is added, and the product precipitates as the hydrochloride salt. Weight of product 0.70 g., m.p. 294-295° dec. Recrystallization from ethanol-water gives 0.45 g. of pure product, m.p. 315-317° dec.
Workup
- additionA mixture of 1.5 g
- filtrationThe catalyst is filtered
- concentrationthe filtrate concentrated to a volume of 50 ml
- additionEthanolic hydrochloric acid is added
- customthe product precipitates as the hydrochloride salt
- customRecrystallization from ethanol-water
- customgives 0.45 g
Sources & evidence
- ORD record
- ord-481645403a0b4a27a3e9eea87bb58719
- Source dataset
- uspto-grants-1978_05
- Patent number
- US04089958
Reaction notes
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