Hydrochloric Acid → 3-amino-8-(2-oxopyrrolidin-1-yl)-1-(thiophen-3-ylmethyl)-3,4-dihydroquinolin-2(1H)-one

Temperature

37.5 °C

tert-Butyl 2-oxo-8-(2-oxopyrrolidin-1-yl)-1-(thiophen-3-ylmethyl)-1,2,3,4-tetrahydroquinolin-3-ylcarbamate (5.0 g) was suspended in ethyl acetate (30 mL), and 4N hydrochloric acid in ethyl acetate (28.3 mL) was added thereto, followed by stirring at 35-40° C. for one hour. The reaction mixture was added to a solution of potassium bicarbonate (11.3 g) in water (20 mL), and the mixture was partitioned at 45° C. The aqueous layer was extracted with ethyl acetate twice, and the organic layers were combined. The combined organic layer was concentrated under reduced pressure until precipitates were formed. The concentrated residue was stirred at room temperature for 30 minutes, and the formed precipitates were recovered through filtration. The thus-obtained solid was washed with ethyl acetate, and then dried under reduced pressure, whereby the title compound (2.93 g) was yielded as crystals.

1. customthe mixture was partitioned at 45° C
2. extractionThe aqueous layer was extracted with ethyl acetate twice
3. concentrationThe combined organic layer was concentrated under reduced pressure
4. customuntil precipitates
5. customwere formed
6. stirringThe concentrated residue was stirred at room temperature for 30 minutes
7. customthe formed precipitates
8. filtrationwere recovered through filtration
9. washThe thus-obtained solid was washed with ethyl acetate
10. dry with materialdried under reduced pressure, whereby the title compound (2.93 g)
11. customwas yielded as crystals

ORD record

ord-4c629df802944c8593f41cf148b5593f

Source dataset

uspto-grants-2013_08

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US08501772B2