Pivaloyl chloride → 1-(1-Naphthalen-1-yl-ethyl)-aziridine-2-carboxylic acid but-3-enyl-phenethyl-amide

HRID 2196829

반응식

HRID 2196829 반응식
CO[C:3]([CH:5]1[CH2:7][N:6]1[CH:8]([C:10]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=[CH:12][CH:11]=1)[CH3:9])=[O:4].O([Si](C)(C)C)[K].CC(C)(C)C(Cl)=O.[CH2:33]([NH:37][CH2:38][CH2:39][C:40]1[CH:45]=[CH:44][CH:43]=[CH:42][CH:41]=1)[CH2:34][CH:35]=[CH2:36].C(=O)(O)[O-].[Na+]>C1COCC1>[CH2:33]([N:37]([CH2:38][CH2:39][C:40]1[CH:41]=[CH:42][CH:43]=[CH:44][CH:45]=1)[C:3]([CH:5]1[CH2:7][N:6]1[CH:8]([C:10]1[C:19]2[C:14](=[CH:15][CH:16]=[CH:17][CH:18]=2)[CH:13]=[CH:12][CH:11]=1)[CH3:9])=[O:4])[CH2:34][CH:35]=[CH2:36]

참가 물질

7

반응물 5

HCID 62493Pivaloyl chlorideHCID 516892Sodium BicarbonateHCID 16720109N-(2-phenylethyl)but-3-en-1-amineHCID 866010811-(1-Naphthalen-1-yl-ethyl)-aziridine-2-carboxylic acid methyl esterHCID 178504318HCID 178504318, 화합물

생성물 1

HCID 866010821-(1-Naphthalen-1-yl-ethyl)-aziridine-2-carboxylic acid but-3-enyl-phenethyl-amide수율 76.4%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

To a solution of 1 (12.6 g, 49.75 mmol) in THF (200 mL) is added KOTMS (6.38 g, 49.75 mmol). The mixture is stirred overnight at room temperature. The mixture is concentrated and the residue dissolved in dichloromethane (200 mL) and cooled to 0° C. Trimethylacetyl chloride (5.94 g, 49.25 mmol) is added slowly and the mixture is warmed to room temperature over 2 hours. The mixture is cooled to −78° C., 2 (8.63 g, 49.25 mmol) is added and stirring continued at −78° C. for 1.5 h. Saturated sodium bicarbonate (100 mL) is added and the mixture is allowed to warm to rt. The mixture is extracted with EtOAc (4×100 mL) and the organic extracts are combined, dried and concentrated under vacuum. The residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8) to provide 15 g (76%) of the title compound as a mixture of two diastereomers in an equimolecular ratio. M+H+=399.37.

후처리

  1. concentrationThe mixture is concentrated
  2. dissolutionthe residue dissolved in dichloromethane (200 mL)
  3. temperaturecooled to 0° C
  4. temperaturethe mixture is warmed to room temperature over 2 hours
  5. temperatureThe mixture is cooled to −78° C.
  6. stirringstirring
  7. waitcontinued at −78° C. for 1.5 h
  8. temperatureto warm to rt
  9. extractionThe mixture is extracted with EtOAc (4×100 mL)
  10. customdried
  11. concentrationconcentrated under vacuum
  12. customThe residue is purified by flash chromatography (silica gel; Hexane/EtOAc 1:8)

출처 및 근거

ORD 기록
ord-7169ec6c35c343c491b32a76fe3a9421
출처 데이터셋
uspto-grants-2012_12
특허 번호
US08338440B2

연결된 노트

불러오는 중…