Dimethyl Sulfoxide → HCID 20694317, compound

Temperature

-78 °C

A solution of 2.04 mL (23.4 mmol) of oxalyl chloride in 40 mL of dry CH2Cl2 was cooled to −78° C. under nitrogen. To this was added 3.32 mL (46.8 mmol) of DMSO and the mixture was stirred at −78° C. for 15 min. A solution of 3.2 g (11.7 mmol) of 1-benzyl-3-(S)-hydroxymethyl-4-(R)-(3-thienyl)pyrrolidine in 20 mL of dry CH2Cl2 was added and the mixture was stirred at −78° C. for 15 min. Then 8.15 mL (58.5 mmol) of triethylamine were added and the solution was allowed to warm to room temperature over 1 h. The reaction mixture was diluted with 400 mL of ether, poured onto 200 mL of water and the layers were separated. The aqueous layer was washed with ether and the combined organic extracts were washed with saturated NaHCO3 solution and brine. The organic fraction was dried over Na2SO4, filtered, and concentrated to afford the title compound, which was used directly in the next step.

1. stirringthe mixture was stirred at −78° C. for 15 min
2. temperatureto warm to room temperature over 1 h
3. customthe layers were separated
4. washThe aqueous layer was washed with ether
5. washthe combined organic extracts were washed with saturated NaHCO3 solution and brine
6. dry with materialThe organic fraction was dried over Na2SO4
7. filtrationfiltered
8. concentrationconcentrated

ORD record

ord-001e532e7b0c4dd79361eb990719fd50

Source dataset

uspto-grants-2001_10

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06303593B1