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

Phosphorus oxychloride → 4-Chloro-6-(4-bromophenyl)thieno[3,2-c]pyridine

HRID 1814496
노트
인쇄 미리보기

반응식

HRID 1814496 반응식
[Br:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[NH:13][C:12](=O)[C:11]3[CH:15]=[CH:16][S:17][C:10]=3[CH:9]=2)=[CH:4][CH:3]=1.P(Cl)(Cl)([Cl:20])=O>>[Cl:20][C:12]1[C:11]2[CH:15]=[CH:16][S:17][C:10]=2[CH:9]=[C:8]([C:5]2[CH:6]=[CH:7][C:2]([Br:1])=[CH:3][CH:4]=2)[N:13]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 24813Phosphorus oxychlorideHCID 225024536-(4-bromophenyl)-5H-thieno[3,2-c]pyridin-4-one

생성물 1

HCID 225035574-Chloro-6-(4-bromophenyl)thieno[3,2-c]pyridine

반응 조건

온도
100 °C

실험 절차

6-(4-Bromophenyl)-5H-thieno[3,2-c]pyridin-4-one (4.87 g) was added to phosphorus oxychloride (30 ml), and the resulting mixture was heated at 100° C. for 3 hr. The reaction solution was evaporated, and to the resulting residue were added ethyl acetate and water. The organic layer was washed with water, an aqueous solution of saturated sodium bicarbonate and brine, and dried over magnesium sulfate. The solvent was evaporated, to give 4-chloro-6-(4-bromophenyl)thieno[3,2-c]pyridine.

후처리

  1. custom
The reaction solution was evaporated
  • additionto the resulting residue were added ethyl acetate and water
  • washThe organic layer was washed with water
  • dry with materialan aqueous solution of saturated sodium bicarbonate and brine, and dried over magnesium sulfate
  • customThe solvent was evaporated
  • 출처 및 근거

    ORD 기록
    ord-495c886d53cc49c48b2a090a71ac7bf2
    출처 데이터셋
    uspto-grants-2005_04
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US06875761B2

    반응 노트

    불러오는 중…

    이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트