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

1H-1,2,4-Triazole → 4-Ethyl-6-(1,2,4-triazol-1-yl)pyrimidine

HRID 850109
노트
인쇄 미리보기

반응식

HRID 850109 반응식
Cl[C:2]1[CH:7]=[C:6]([CH2:8][CH3:9])[N:5]=[CH:4][N:3]=1.[NH:10]1[CH:14]=[N:13][CH:12]=[N:11]1>CO.ClCCl>[CH2:8]([C:6]1[CH:7]=[C:2]([N:10]2[CH:14]=[N:13][CH:12]=[N:11]2)[N:3]=[CH:4][N:5]=1)[CH3:9]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 2

HCID 92571H-1,2,4-TriazoleHCID 111372714-Chloro-6-ethylpyrimidine

생성물 1

HCID 193659594-Ethyl-6-(1,2,4-triazol-1-yl)pyrimidine수율 82.2%

시약·촉매·용매 2

HCID 887Methanol용매HCID 6344Dichloromethane용매

반응 조건

온도
120 °C

실험 절차

A mixture of 4-chloro-6-ethylpyrimidine (1.42 g, 10 mmol) and 1H-1,2,4-triazole (1.4 g, 20 mmol) was heated to 120° C. with stirring to give a yellow oil, which deposited an orange solid. The mixture was maintained at 120° C. for 0.2 hours, cooled to 70° C. and dissolved in methanol (10 ml). The solution was diluted with dichloromethane (50 ml) and was washed with saturated sodium bicarbonate solution (20 ml). The aqueous phase was extracted with dichloromethane (2×20 ml) and the combined organic layers were dried (MgSO4) and evaporated under reduced pressure. The crude product was purified by column chromatography on silica by elution with ethyl acetate to give the title compound (1.44 g, 82%) as a yellow solid, m.p. 75-76° C., which was characterised by 1H-N.M.R. spectroscopy.

후처리

  1. customto give a yellow oil, which
  2. temperatureThe mixture was maintained at 120° C. for 0.2 hours
  3. temperaturecooled to 70° C.
  4. washwas washed with saturated sodium bicarbonate solution (20 ml)
  5. extractionThe aqueous phase was extracted with dichloromethane (2×20 ml)
  6. dry with materialthe combined organic layers were dried (MgSO4)
  7. customevaporated under reduced pressure
  8. customThe crude product was purified by column chromatography on silica by elution with ethyl acetate

출처 및 근거

ORD 기록
ord-f25f375d64184046b6faf5983d5f1c54
출처 데이터셋
uspto-grants-2000_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06015825

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트