Hydrochloric Acid → HCID 20339412, compound
Reaction equation
[F:1][C:2]([F:19])([F:18])[C:3]1[CH:4]=[C:5]2[C:10](=[CH:11][CH:12]=1)[N:9]1[CH2:13][CH2:14][NH:15][CH2:16][CH:8]1[C:7](=[O:17])[NH:6]2.[CH:20]([C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][N:23]=1)=[CH2:21].CO.Cl>C(O)C.C(O)(=O)C>[N:23]1[CH:24]=[CH:25][CH:26]=[CH:27][C:22]=1[CH2:20][CH2:21][N:15]1[CH2:14][CH2:13][N:9]2[C:10]3[C:5]([NH:6][C:7](=[O:17])[CH:8]2[CH2:16]1)=[CH:4][C:3]([C:2]([F:18])([F:1])[F:19])=[CH:12][CH:11]=3Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 2
Procedure
A solution of 8.5 g. (0.03 mole) of 2,3,4,4a-tetrahydro-8-trifluoromethyl-1H-pyrazino[1,2-a]quinoxalin-5(6H)-one and 17.5 g. (0.16 mole) of 2-vinylpyridine in 250 ml. of methanol containing 7 ml. acetic acid was heated under reflux for 20 hours. The reaction mixture was cooled, and the solvent was removed under reduced pressure. The residue was precipitated with 1 l. of water. The product was filtered and recrystallized from methanol-water to yield 10.1 g. of free base. 4.5 G. of this free base was dissolved in 150 ml. of absolute ethanol and treated with dry hydrogen chloride saturated ether solution. The product hydrochloride was filtered and recrystallized two times from methanol-ether to give 4 g. (71%) of the title compound as the dihydrochloride salt, m.p. 194°-196° C.
Workup
- temperatureunder reflux for 20 hours
- temperatureThe reaction mixture was cooled
- customthe solvent was removed under reduced pressure
- customThe residue was precipitated with 1 l
- filtrationThe product was filtered
- customrecrystallized from methanol-water
- customto yield 10.1 g
- dissolutionof this free base was dissolved in 150 ml
- filtrationThe product hydrochloride was filtered
- customrecrystallized two times from methanol-ether
- customto give 4 g
Sources & evidence
- ORD record
- ord-957a35fd298a4cc28c3e29bf5720b8a3
- Source dataset
- uspto-grants-1980_05
- Patent number
- US04203987
Reaction notes
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