Triethylamine → Ethyl 2-(cyclobutanecarboxamido)-3-mercaptopropanoate

HRID 1689347

반응식

HRID 1689347 반응식
C(N(CC)CC)C.[CH:8]1([C:12]([OH:14])=O)[CH2:11][CH2:10][CH2:9]1.Cl.[NH2:16][CH:17]([CH2:23][SH:24])[C:18]([O:20][CH2:21][CH3:22])=[O:19].C(P1(=O)OP(CCC)(=O)OP(CCC)(=O)O1)CC>CN(C=O)C>[CH:8]1([C:12]([NH:16][CH:17]([CH2:23][SH:24])[C:18]([O:20][CH2:21][CH3:22])=[O:19])=[O:14])[CH2:9][CH2:10][CH2:11]1

참가 물질

6

실험 절차

Triethylamine (15 mL) was added to a suspension of cyclobutanecarboxylic acid (2.57 mL) and ethyl 2-amino-3-mercaptopropanoate hydrochloride (5 g) in DMF (40 mL). The resulting mixture was cooled in an ice bath and a solution of T3P (1.57M in THF, 20.6 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 clear oil. Yield 3.20 g.

후처리

  1. temperatureThe resulting mixture was cooled in an ice 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-7bc51379fc2341fa944fc16a1a64dd03
출처 데이터셋
uspto-grants-2012_04
특허 번호
US08148373B2

연결된 노트

불러오는 중…