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

Dimethylformamide → HCID 20563001, 화합물

HRID 613980
노트
인쇄 미리보기

반응식

HRID 613980 반응식
N[C:2]1[O:3][C:4]2[CH:14]=[CH:13][C:12]([CH2:15][CH3:16])=[CH:11][C:5]=2[C:6](=[O:10])[C:7]=1C=O.[C:17]([CH2:19][C:20](Cl)=O)#[N:18].C[N:24]([CH3:27])C=O>>[CH2:15]([C:12]1[CH:11]=[C:5]2[C:4]([O:3][C:2]3[CH:20]=[C:19]([C:27]#[N:24])[CH:17]=[N:18][C:7]=3[C:6]2=[O:10])=[CH:14][CH:13]=1)[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 3

HCID 6228DimethylformamideHCID 110515942-Cyanoacetyl chlorideHCID 126892482-Amino-6-ethyl-4-oxo-4H-1-benzopyran-3-carbaldehyde

생성물 1

HCID 20563001HCID 20563001, 화합물

실험 절차

In 40 ml of dimethylformamide was dissolved 1.82 g of 2-amino-6-ethyl-4-oxo-4H-1-benzopyran-3-carboxaldehyde, followed by the addition of 3.5 g of cyanoacetyl chloride. The mixture was reacted at 60° C. for 3 hours, with constant stirring. The solvent was then distilled off under reduced pressure and the residue was chromatographed on silica gel. The desired product was recovered from the chloroform eluate and recrystallized from acetonitrile. By the above procedure was obtained 1.03 g of 7-ethyl-3-cyano-1-azaxanthone, m.p. 183°-185° C.

후처리

  • customThe mixture was reacted at 60° C. for 3 hours, with constant stirring
  • distillationThe solvent was then distilled off under reduced pressure
  • customthe residue was chromatographed on silica gel
  • customThe desired product was recovered from the chloroform eluate
  • customrecrystallized from acetonitrile
  • 출처 및 근거

    ORD 기록
    ord-647ff5ea3541436486f751158bb8f76d
    출처 데이터셋
    uspto-grants-1979_03
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US04143042

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트