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

Toluene → 5-Chloropyrido[3,4-b]pyrazin-2(1H)-one

HRID 627610
노트
인쇄 미리보기

반응식

HRID 627610 반응식
[Cl:1][C:2]1[C:7]([NH2:8])=[C:6]([NH2:9])[CH:5]=[CH:4][N:3]=1.[C:10](OCC)(=O)[CH:11]=[O:12].C1(C)C=CC=CC=1>C(O)C>[Cl:1][C:2]1[C:7]2[N:8]=[CH:10][C:11](=[O:12])[NH:9][C:6]=2[CH:5]=[CH:4][N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 1140TolueneHCID 70211Ethyl oxoacetateHCID 2857362-Chloropyridine-3,4-diamine

생성물 1

HCID 867157425-Chloropyrido[3,4-b]pyrazin-2(1H)-one

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
-20 °C

실험 절차

A suspension 2-chloropyridine-3,4-diamine (2.5 g, 17.41 mmol) and a 50% solution of ethyl glyoxalate in toluene (3.45 mL, 17.41 mmol) in ethanol (34.8 mL) was stirred at reflux for 24 hours. The solution was cooled to −20° C. for 16 hours, and the resulting precipitate was collected by vacuum filtration and rinsed with ethanol. The crude product was purified via reverse-phase HPLC, eluting with 5-50% acetonitrile/0.1% trifluoroacetic acid in water/0.1% trifluoroacetic acid, to afford the title compound (570 mg, 3.14 mmol). MS m/z=182 (M+H).

후처리

  1. temperatureat reflux for 24 hours
  2. filtrationthe resulting precipitate was collected by vacuum filtration
  3. washrinsed with ethanol
  4. customThe crude product was purified via reverse-phase HPLC
  5. washeluting with 5-50% acetonitrile/0.1% trifluoroacetic acid in water/0.1% trifluoroacetic acid

출처 및 근거

ORD 기록
ord-e9ee707b04cb45c28ecff6ed49c8237b
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09309263B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트