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

Dimethyl Sulfoxide → 2-(2-Azido-1,1-difluoro-ethyl)-pyrimidine

HRID 1171071
노트
인쇄 미리보기

반응식

HRID 1171071 반응식
[F:1][C:2]([C:6]1[N:11]=[CH:10][CH:9]=[CH:8][N:7]=1)([F:5])[CH2:3]I.[N-:12]=[N+:13]=[N-:14].[Na+].CS(C)=O>O>[N:12]([CH2:3][C:2]([C:6]1[N:11]=[CH:10][CH:9]=[CH:8][N:7]=1)([F:5])[F:1])=[N+:13]=[N-:14]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 679Dimethyl SulfoxideHCID 33557Sodium AzideHCID 58973005Pyrimidine, 2-(1,1-difluoro-2-iodoethyl)-

생성물 1

HCID 866153122-(2-Azido-1,1-difluoro-ethyl)-pyrimidine수율 102.6%

시약·촉매·용매 1

HCID 962Water용매

반응 조건

온도
95 °C

실험 절차

A mixture of 2-(1,1-difluoro-2-iodo-ethyl)-pyrimidine (841 mg, 3.11 mmol), as prepared in the previous step, NaN3 (338 mg, 5.19 mmol), and DMSO (2.35 mL) was stirred at 95° C. for 3 days. The reaction was then shaken with water (10 mL) and extracted with ether (3×8 mL). The organic layers were combined, dried (Na2SO4), and concentrated to give the intermediate 2-(2-azido-1,1-difluoro-ethyl)-pyrimidine as a clear yellow oil (591 mg) that was immediately used in the next step without further purification or characterization.

후처리

  1. extractionextracted with ether (3×8 mL)
  2. dry with materialdried (Na2SO4)
  3. concentrationconcentrated

출처 및 근거

ORD 기록
ord-0725ab80f1fa456d891d9fd65f047081
출처 데이터셋
uspto-grants-2010_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07829584B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트