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

Sodium Carbonate → (2R,5S)-Dimethyl 1-(2-(1,3-dioxoisoindolin-2-yl)ethyl)piperidine-2,5-dicarboxylate

HRID 466583
노트
인쇄 미리보기

반응식

HRID 466583 반응식
C(=O)([O-])[O-].[Na+].[Na+].Cl.[CH3:8][O:9][C:10]([C@H:12]1[CH2:17][CH2:16][C@H:15]([C:18]([O:20][CH3:21])=[O:19])[CH2:14][NH:13]1)=[O:11].O([CH2:30][CH2:31][N:32]1[C:36](=[O:37])[C:35]2=[CH:38][CH:39]=[CH:40][CH:41]=[C:34]2[C:33]1=[O:42])S(C(F)(F)F)(=O)=O>O.C(Cl)Cl>[C:33]1(=[O:42])[N:32]([CH2:31][CH2:30][N:13]2[CH2:14][C@@H:15]([C:18]([O:20][CH3:21])=[O:19])[CH2:16][CH2:17][C@@H:12]2[C:10]([O:9][CH3:8])=[O:11])[C:36](=[O:37])[C:35]2=[CH:38][CH:39]=[CH:40][CH:41]=[C:34]12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 3

HCID 10340Sodium CarbonateHCID 118094652-(1,3-Dioxoisoindolin-2-yl)ethyl trifluoromethanesulfonateHCID 67703709trans-2,5-Piperidine dicarboxylate dimethyl ester hydrochloride

생성물 1

HCID 21782948(2R,5S)-Dimethyl 1-(2-(1,3-dioxoisoindolin-2-yl)ethyl)piperidine-2,5-dicarboxylate수율 99.1%

시약·촉매·용매 2

HCID 962
Water
용매
HCID 6344Dichloromethane용매2회

실험 절차

To a well-stirred bi-phasic mixture consisting of sodium carbonate (500 g, 4.72 mol) in water (3 liters) and trans-2,5-piperidine dicarboxylate dimethyl ester hydrochloride (280 g, 1.18 mol) in methylene chloride (4.5 liters), a solution of 2-phthalimido-ethyl triflate (417 g, 1.29 mol) in methylene chloride (3 liters) was added in a steady stream over a 3 hour period. The organic layer was separated, and the aqueous layer was extracted with fresh methylene chloride (3 liters). The combined organic extracts were washed with water (3 liters), then with brine (3 liters), dried with anhydrous magnesium sulfate and finally, concentrated in vacuo to a solid. The entire residue was triturated in refluxing ether (3 liters), with vigorous stirring, for 15 minutes. After cooling to ambient temperature, the solution was poured into hexanes (3 liters), and the resulting mixture was stirred for 18 hours. The resulting colorless solid was collected by filtration, and the filter cake was washed with hexanes (1 liter). In vacuo drying afforded 437.3 g (99.1% yield) of the title compound as a colorless solid. TLC Rf (ethyl acetate/methylene chloride=1:1 in volume; iodoplatinate spray): 0.5.

후처리

  1. customThe organic layer was separated
  2. extractionthe aqueous layer was extracted with fresh methylene chloride (3 liters)
  3. washThe combined organic extracts were washed with water (3 liters)
  4. dry with materialwith brine (3 liters), dried with anhydrous magnesium sulfate
  5. concentrationfinally, concentrated in vacuo to a solid
  6. customThe entire residue was triturated
  7. temperaturein refluxing ether (3 liters)
  8. additionthe solution was poured into hexanes (3 liters)
  9. filtrationThe resulting colorless solid was collected by filtration
  10. washthe filter cake was washed with hexanes (1 liter)
  11. customIn vacuo drying

출처 및 근거

ORD 기록
ord-ae16a20788bc4fb38ec15ba3ae8634ad
출처 데이터셋
uspto-grants-1992_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05157034

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트