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

Lithium hydroxide, monohydrate → (R)-Quinuclidin-3-yl((3-(3-hydroxypropoxy)phenyl)(phenyl)methyl)carbamate

HRID 332707
노트
인쇄 미리보기

반응식

HRID 332707 반응식
C([O:9][CH2:10][CH2:11][CH2:12][O:13][C:14]1[CH:19]=[CH:18][CH:17]=[C:16]([CH:20]([C:33]2[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=2)[NH:21][C:22]([O:24][C@@H:25]2[CH:30]3[CH2:31][CH2:32][N:27]([CH2:28][CH2:29]3)[CH2:26]2)=[O:23])[CH:15]=1)(=O)C1C=CC=CC=1.O.[OH-].[Li+]>CO.O>[N:27]12[CH2:28][CH2:29][CH:30]([CH2:31][CH2:32]1)[C@@H:25]([O:24][C:22](=[O:23])[NH:21][CH:20]([C:16]1[CH:17]=[CH:18][CH:19]=[C:14]([O:13][CH2:12][CH2:11][CH2:10][OH:9])[CH:15]=1)[C:33]1[CH:34]=[CH:35][CH:36]=[CH:37][CH:38]=1)[CH2:26]2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 168937Lithium hydroxide, monohydrate2회HCID 710930683-(3-(phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)-methyl)phenoxy)propyl benzoate

생성물 1

HCID 117680437(R)-Quinuclidin-3-yl((3-(3-hydroxypropoxy)phenyl)(phenyl)methyl)carbamate수율 93%

시약·촉매·용매 2

HCID 887Methanol용매HCID 962Water
용매

실험 절차

To a stirred solution of 3-(3-(phenyl((((R)-quinuclidin-3-yloxy)carbonyl)amino)-methyl)phenoxy)propyl benzoate (0.370 g, 0.72 mmol) in methanol (3.6 mL), was added a solution of lithium hydroxide monohydrate (0.060 g, 1.44 mmol) in water (1.2 mL). The reaction mixture was stirred at room temperature for 1 hour. Further lithium hydroxide monohydrate (0.060 g, 1.44 mmol) was added, and the reaction stirred at room temperature for a further 16 hours. The reaction mixture was heated at 40° C. for 3.5 hours and allowed to cool. The solvent was evaporate at reduced pressure, and the residue partitioned between ethyl acetate and water. The aqueous phase was further extracted with ethyl acetate (×2). The combined organic extracts were washed with 10% aqueous potassium carbonate (×2), saturated brine, and dried with anhydrous sodium sulfate. The mixture was filtered and the solvent evaporated at reduced pressure to afford the title compound (0.275 g, 93%).

후처리

  1. stirringthe reaction stirred at room temperature for a further 16 hours
  2. temperatureThe reaction mixture was heated at 40° C. for 3.5 hours
  3. temperatureto cool
  4. customThe solvent was evaporate at reduced pressure
  5. customthe residue partitioned between ethyl acetate and water
  6. extractionThe aqueous phase was further extracted with ethyl acetate (×2)
  7. washThe combined organic extracts were washed with 10% aqueous potassium carbonate (×2), saturated brine
  8. dry with materialdried with anhydrous sodium sulfate
  9. filtrationThe mixture was filtered
  10. customthe solvent evaporated at reduced pressure

출처 및 근거

ORD 기록
ord-ef77d7bb14e74f828fcc2cf5570dba00
출처 데이터셋
uspto-grants-2014_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08877774B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트