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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Ammonia → 2-Amino-4-fluoro-6-trifluoromethoxypyrimidine

HRID 1647677
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인쇄 미리보기

반응식

HRID 1647677 반응식
[NH3:1].F[C:3]1[N:8]=[C:7]([F:9])[CH:6]=[C:5]([O:10][C:11]([F:14])([F:13])[F:12])[N:4]=1>C(OCC)C>[NH2:1][C:3]1[N:8]=[C:7]([F:9])[CH:6]=[C:5]([O:10][C:11]([F:14])([F:13])[F:12])[N:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 150227122,4-Difluoro-6-trifluoromethoxypyrimidine

생성물 1

HCID 150227162-Amino-4-fluoro-6-trifluoromethoxypyrimidine

시약·촉매·용매 1

HCID 3283Diethyl Ether용매

실험 절차

8.7 g (0.51 mol) of gaseous ammonia were passed into a mixture of 51 g (0.255 mol) of 2,4-difluoro-6-trifluoromethoxypyrimidine in 200 ml of diethyl ether in the course of 1 hour at from -75° to -70° C. while stirring. Stirring was continued for a further 11/2 hours at -70° C. and for 1 hour at room temperature. The reaction mixture was evaporated down under reduced pressure and the residue was taken up in methylene chloride and extracted with water. Drying the organic phase, evaporating down and chromatographing the residue over silica gel using 8:1 petroleum ether/ether gave 38.1 g (75.6% of theory) of the title compound as colorless crystals of melting point 86°-89° C.

후처리

  1. stirringStirring
  2. custom2 hours
  3. customat -70° C.
  4. customThe reaction mixture was evaporated down under reduced pressure
  5. extractionextracted with water
  6. customDrying the organic phase
  7. customevaporating down

출처 및 근거

ORD 기록
ord-9e9520d88ad64317bb0f656f90064e5f
출처 데이터셋
uspto-grants-1995_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05434124

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