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

3,6-Dichloropyridazine → 6-Chloro-N-methylpyridazin-3-amine

HRID 454824
노트
인쇄 미리보기

반응식

HRID 454824 반응식
[Cl:1][C:2]1[N:3]=[N:4][C:5](Cl)=[CH:6][CH:7]=1.CO.[CH3:11][NH2:12]>O>[CH3:11][NH:12][C:5]1[N:4]=[N:3][C:2]([Cl:1])=[CH:7][CH:6]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 673313,6-DichloropyridazineHCID 57454252Monomethylamine methanol

생성물 1

HCID 5885406-Chloro-N-methylpyridazin-3-amine수율 104.7%

시약·촉매·용매 1

HCID 962Water용매

실험 절차

3,6-Dichloropyridazine (107, 500 mg, 3.36 mmol) was slowly added to a 2.0 M methylamine methanol solution (NH2Me in MeOH, 5 mL, 10 mmol) and stirred at room temperature for 24 hours. Water was added to the reaction mixture, and organic compounds were extracted with ethyl acetate. The recovered organic solution was washed with an aqueous solution of saturated sodium chloride and evaporated after a treatment with sodium sulfate. Purification was performed by column chromatograph to give the target compound 3-(N-monomethylamino)-6-chloropyridazine (108e, 505 mg, 88%) as a white solid.

후처리

  1. extractionwere extracted with ethyl acetate
  2. washThe recovered organic solution was washed with an aqueous solution of saturated sodium chloride
  3. customevaporated after a treatment with sodium sulfate
  4. customPurification

출처 및 근거

ORD 기록
ord-171ec25a3f954b868203a18a0508ed80
출처 데이터셋
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08497260B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트