1-Chloroethyl chloroformate → 3-[(1R)-1-cyclopropylethoxy]-6,7,8,9-tetrahydropyrazino[2,3-f][1,4]oxazepine hydrochloride

Temperatur

90 °C

To a solution of 8-benzyl-3-[(1R)-1-cyclopropylethoxy]-6,7,8,9-tetrahydropyrazino[2,3-f][1,4]oxazepine (32.9 mg) in toluene (3 mL) was added 1-chloroethyl chloroformate (0.11 mL), and the mixture was stirred at 90° C. for 3 hr. The reaction mixture was cooled to room temperature, and concentrated. To the obtained residue was added methanol (3 mL), and the mixture was stirred at 60° C. for 1 hr. The reaction mixture was cooled to room temperature, and concentrated. The concentrate was diluted with ethyl acetate, and washed with saturated aqueous sodium hydrogen carbonate, water and saturated brine. The organic layer was dried over anhydrous magnesium sulfate, and concentrated under reduced pressure. The obtained residue was purified by basic silica gel column chromatography (solvent gradient; 10→100% ethyl acetate/hexane). To a solution of the obtained oil in methanol (1 mL) was added 1 N hydrochloric acid (0.45 mL), and the mixture was concentrated under reduced pressure. The obtained crude crystals were purified by recrystallization (ethanol-diisopropyl ether) to give the title compound (8.6 mg, 3%) as colorless crystals.

1. temperatureThe reaction mixture was cooled to room temperature
2. concentrationconcentrated
3. additionTo the obtained residue was added methanol (3 mL)
4. stirringthe mixture was stirred at 60° C. for 1 hr
5. temperatureThe reaction mixture was cooled to room temperature
6. concentrationconcentrated
7. additionThe concentrate was diluted with ethyl acetate
8. washwashed with saturated aqueous sodium hydrogen carbonate, water and saturated brine
9. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
10. concentrationconcentrated under reduced pressure
11. customThe obtained residue was purified by basic silica gel column chromatography (solvent gradient; 10→100% ethyl acetate/hexane)
12. additionTo a solution of the obtained oil in methanol (1 mL) was added 1 N hydrochloric acid (0.45 mL)
13. concentrationthe mixture was concentrated under reduced pressure
14. customThe obtained crude crystals
15. customwere purified by recrystallization (ethanol-diisopropyl ether)

ORD-Eintrag

ord-31f26b024ab24c068e7917f3b038dee4

Quelldatensatz

uspto-grants-2012_11

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08314088B2