반응 #166871

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Sodium triacetoxyborohydride

5-formyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

glycine t-butyl ester

→

5-[(tert-butoxycarbonylmethyl-amino)-methyl]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester

수율 47.1%

용매

dichloromethane

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후처리

1. 1
   기타After 1 hour the reaction was quenched with saturated ammonium chloride (5 mL)
2. 2
   추출The mixture was extracted with ethyl acetate (3×25 mL)
3. 3
   건조The combined organic phases were dried over sodium sulfate
4. 4
   여과filtered
5. 5
   기타the solvent was removed under reduced pressure
6. 6
   기타The resulting residue was purified by flash chromatography with methanol and dichloromethane as the eluant at a gradient of 0-10%
7. 7
   workup.ADDITIONThe fractions containing product
8. 8
   기타the solvent was removed under reduced pressure

실험 절차

Sodium triacetoxyborohydride (2.08 g, 9.86 mmol) was added to a solution of 5-formyl-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (891 mg, 3.29 mmol) and glycine t-butyl ester (1.65 g, 9.86 mmol) in dichloromethane (20 mL) over 2 minutes—a small amount of gas evolution was observed. After 1 hour the reaction was quenched with saturated ammonium chloride (5 mL). The mixture was extracted with ethyl acetate (3×25 mL). The combined organic phases were dried over sodium sulfate, filtered and the solvent was removed under reduced pressure. The resulting residue was purified by flash chromatography with methanol and dichloromethane as the eluant at a gradient of 0-10%. The fractions containing product were combined and the solvent was removed under reduced pressure to provide 5-[(tert-butoxycarbonylmethyl-amino)-methyl]-pyrrolidine-1,2-dicarboxylic acid 1-tert-butyl ester 2-ethyl ester (601 mg, 1.55 mmol, 47%). C19H34N2O6 calculated 386.2, observed [M+1]+ 387.2; rt=1.61 min.

출처