홈MCP워크벤치Skills
홈워크벤치알림마이페이지
llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
  1. 홈
  2. /반응

(3S,4S)-4-(1-chloromethylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone → HCID 15000239, 화합물

HRID 1196202
노트
인쇄 미리보기

반응식

HRID 1196202 반응식
[Cl:1][CH2:2][C:3]([C@H:5]1[N:8](C(CC2C=CC(OC)=CC=2)CC2C=CC(OC)=CC=2)[C:7](=[O:28])[C@@H:6]1[C@H:29]([O:31][C:32]([O:34][CH2:35][C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1)=[O:33])[CH3:30])=[CH2:4]>C(#N)C.O.CO>[Cl:1][CH2:2][C:3]([C@H:5]1[NH:8][C:7](=[O:28])[C@@H:6]1[C@H:29]([O:31][C:32]([O:34][CH2:35][C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1)=[O:33])[CH3:30])=[CH2:4]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 1

HCID 67796056(3S,4S)-4-(1-chloromethylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone

생성물 1

HCID 15000239HCID 15000239, 화합물

시약·촉매·용매 3

HCID 887Methanol용매HCID 962Water용매3회HCID 6342Acetonitrile용매2회

실험 절차

To a solution of (3S,4S)-4-(1-chloromethylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-1-di(p-anisyl)methyl-2-azetidinone (320 g) in a mixture of acetonitrile and water (9 : 1) (3.8 liters) was added a solution of ceric ammonium nitrate (702 g) in a mixture of acetonitrile and water (9 : 1) (2 liters) at 5° C. or lower, followed by stirring for 30 minutes. The reaction mixture was diluted with water (5.2 liters) and extracted with ethyl acetate (3.4 liters). The aqueous layer was extracted with a mixture of ethyl acetate (1.7 liters), diethyl ether (1.7 liters) and benzene (1.7 liters). The combined extracts were washed successively with brine, 5l% sodium bicarbonate and brine, and dried over anhydrous sodium sulfate. Filtration and concentration of the filtrate in vacuo gave an oily residue, which was dissolved in methanol (1.5 liters) with warming and allowed to cool gradually. After filtration to remove crystals, the filtrate was concentrated in vacuo to give an oily residue, which was purified by silica gel chromatography to yield (3S,4S)-4-(1-chloromethylethenyl)-3-(1-(R)-benzyloxycarbonyloxyethyl)-2-azetidinone.

후처리

  1. extractionextracted with ethyl acetate (3.4 liters)
  2. extractionThe aqueous layer was extracted with a mixture of ethyl acetate (1.7 liters), diethyl ether (1.7 liters) and benzene (1.7 liters)
  3. washThe combined extracts were washed successively with brine, 5l% sodium bicarbonate and brine
  4. dry with materialdried over anhydrous sodium sulfate
  5. filtrationFiltration and concentration of the filtrate in vacuo
  6. customgave an oily residue, which
  7. temperaturewith warming
  8. temperatureto cool gradually
  9. filtrationAfter filtration
  10. customto remove crystals
  11. concentrationthe filtrate was concentrated in vacuo
  12. customto give an oily residue, which
  13. customwas purified by silica gel chromatography

출처 및 근거

ORD 기록
ord-f666dc010bfb45928b69457a37f09327
출처 데이터셋
uspto-grants-1992_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05112966

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트