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

1,8-Diazabicyclo(5.4.0)undec-7-ene → HCID 86695586, 화합물

HRID 1465720
노트
인쇄 미리보기

반응식

HRID 1465720 반응식
CS(O[CH:6]1[CH2:12][C@@H:11]2[N:13]([C:14]([O:16][C:17]([CH3:20])([CH3:19])[CH3:18])=[O:15])[C@@H:8]([CH2:9][CH2:10]2)[CH:7]1[C:21]([O:23][CH3:24])=[O:22])(=O)=O.C1CCN2C(=NCCC2)CC1>CN(C=O)C>[C@H:8]12[N:13]([C:14]([O:16][C:17]([CH3:18])([CH3:19])[CH3:20])=[O:15])[C@H:11]([CH2:10][CH2:9]1)[CH2:12][CH:6]=[C:7]2[C:21]([O:23][CH3:24])=[O:22]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 811841,8-Diazabicyclo(5.4.0)undec-7-eneHCID 86695585HCID 86695585, 화합물

생성물 1

HCID 86695586HCID 86695586, 화합물수율 52.1%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

(1S,5R)-8-tert-butyl 2-methyl 3-(methylsulfonyloxy)-8-azabicyclo[3.2.1]octane-2,8-dicarboxylate (14.22 g, 39.15 mmol) and DBU (58.55 mL, 391.15 mmol) in DMF (73.87 mL) were heated at 100° C. for 10 hours. The reaction was quenched with saturated sodium bicarbonate solution and extracted with ethyl acetate. The organic fractions were combined, dried with sodium sulfate and concentrated to give crude product. The crude was purified using flash chromatography (0-100% Ethyl Acetate in Hexane) to give 5.45 g of (1S,5R)-8-tert-butyl 2-methyl 8-azabicyclo[3.2.1]oct-2-ene-2,8-dicarboxylate.

후처리

  1. customThe reaction was quenched with saturated sodium bicarbonate solution
  2. extractionextracted with ethyl acetate
  3. dry with materialdried with sodium sulfate
  4. concentrationconcentrated
  5. customto give crude product
  6. customThe crude was purified

출처 및 근거

ORD 기록
ord-3a2e125def8e4671a1c78a6d4203f649
출처 데이터셋
uspto-grants-2015_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08999966B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트