Dimethyl Sulfoxide → methyl 4-({2-[(2R)-2-formyl-5-oxopyrrolidin-1-yl]ethyl}thio)butanoate

A solution of anhydrous dimethylsulfoxide (0.21 mL, 2.7 mmol) in 5 mL of methylene chloride under argon atmosphere was cooled to −70° C. and trifluoroacetic anhydride (0.17 mL, 1.2 mmol) in 1 mL of methylene chloride was added dropwise. The reaction was stirred for 15 minutes maintaining the temperature and then methyl 4-({2-[(5R)-5-(hydroxymethyl)-2-oxo pyrrolidin-1-yl]ethyl}thio)butanoate (0.15 g, 0.55 mmol) in 2 mL of methylene chloride was added. The solution was stirred and kept at −70° C. for 20 minutes followed by the addition of triethylamine (0.27 mL, 1.9 mmol). The reaction was allowed to come to room temperature, stirred for 30 minutes and then quenched with the addition of aqueous phosphoric acid solution (2%, 50 mL) and methylene chloride (25 mL). The reaction phases were separated and the combined organic layers were dried (Na2SO4) and evaporated under reduced pressure to yield methyl 4-({2-[(2R)-2-formyl-5-oxopyrrolidin-1-yl]ethyl}thio)butanoate which was taken on to next step.

1. temperaturemaintaining the temperature
2. stirringThe solution was stirred
3. waitkept at −70° C. for 20 minutes
4. customto come to room temperature
5. stirringstirred for 30 minutes
6. customquenched with the addition of aqueous phosphoric acid solution (2%, 50 mL) and methylene chloride (25 mL)
7. customThe reaction phases were separated
8. dry with materialthe combined organic layers were dried (Na2SO4)
9. customevaporated under reduced pressure

ORD record

ord-23bacf98e1b9453698a29068410ece36

Source dataset

uspto-grants-2005_02

DOI

10.6084/m9.figshare.5104873.v1

Patent number

US06849657B2