Triethylamine → Ethyl 2-butyramido-3-mercaptopropanoate

HRID 471110

반응식

HRID 471110 반응식
C(N(CC)CC)C.Cl.[NH2:9][CH:10]([CH2:16][SH:17])[C:11]([O:13][CH2:14][CH3:15])=[O:12].[C:18](Cl)(=[O:22])[CH2:19][CH2:20][CH3:21]>C(Cl)Cl>[C:18]([NH:9][CH:10]([CH2:16][SH:17])[C:11]([O:13][CH2:14][CH3:15])=[O:12])(=[O:22])[CH2:19][CH2:20][CH3:21]

참가 물질

5

실험 절차

Triethylamine (4.5 mL) was added to a suspension of ethyl 2-amino-3-mercaptopropanoate hydrochloride (5 g) in DCM (50 mL). The resulting mixture was cooled in an ice/salt bath and butyryl chloride (3.3 mL) was added dropwise. The resulting mixture was allowed to warm to RT and stirred overnight. The reaction was quenched with saturated sodium bicarbonate solution (50 mL) and the layers separated. The aqueous phase was extracted with DCM (2×100 mL). The combined organic solutions were washed with brine (100 mL), dried over sodium sulphate, filtered and evaporated. The resulting white solid was purified by silica gel chromatography eluting with 4:1 to 1:1 isohexane:ethyl acetate gradient. The fractions containing product were combined and evaporated to give the subtitled compound as a white solid. Yield 3 g.

후처리

  1. temperatureThe resulting mixture was cooled in an ice/salt bath
  2. customThe reaction was quenched with saturated sodium bicarbonate solution (50 mL)
  3. customthe layers separated
  4. extractionThe aqueous phase was extracted with DCM (2×100 mL)
  5. washThe combined organic solutions were washed with brine (100 mL)
  6. dry with materialdried over sodium sulphate
  7. filtrationfiltered
  8. customevaporated
  9. customThe resulting white solid was purified by silica gel chromatography
  10. washeluting with 4:1 to 1:1 isohexane
  11. additionThe fractions containing product
  12. customevaporated

출처 및 근거

ORD 기록
ord-cccef92026d74d02a6f8ea601a72ac25
출처 데이터셋
uspto-grants-2014_01
특허 번호
US08629271B2

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