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

Water → Ethyl 2,3-dimethylquinoxaline-6-carboxylate

HRID 1498902
노트
인쇄 미리보기

반응식

HRID 1498902 반응식
[NH2:1][C:2]1[CH:3]=[C:4]([CH:10]=[CH:11][C:12]=1[NH2:13])[C:5]([O:7][CH2:8][CH3:9])=[O:6].O>C(O)C>[CH3:3][C:2]1[C:12]([CH3:11])=[N:1][C:2]2[C:12](=[CH:11][CH:10]=[C:4]([C:5]([O:7][CH2:8][CH3:9])=[O:6])[CH:3]=2)[N:13]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 962WaterHCID 458855Ethyl 3,4-Diaminobenzoate

생성물 1

HCID 2826621Ethyl 2,3-dimethylquinoxaline-6-carboxylate수율 203.8%

시약·촉매·용매 1

HCID 702Ethanol용매

실험 절차

Ethyl 3,4-diaminobenzoate (500 mg, 2.77 mmol) and diacetyl (238 mg, 2.77 mmol) were dissolved in ethanol (20 ml), and the mixture was heated under reflux. One hour after, diacetyl (30 mg) was added thereto, and the mixture was heated under reflux. After the mixture was heated under reflux for 2.5 hours in total, the reaction solution was poured into water, and the precipitate was separated by filtration and washed with water. By through circulation drying for 15 hours, the title compound (650 mg, quantitative) as a light-brown powder was obtained.

후처리

  1. temperaturethe mixture was heated
  2. temperatureunder reflux
  3. additionOne hour after, diacetyl (30 mg) was added
  4. temperaturethe mixture was heated
  5. temperatureunder reflux
  6. temperatureAfter the mixture was heated
  7. temperatureunder reflux for 2.5 hours in total, the reaction solution
  8. customthe precipitate was separated by filtration
  9. washwashed with water
  10. customBy through circulation drying for 15 hours

출처 및 근거

ORD 기록
ord-f07b1b93eab54beaad10684964d97d1c
출처 데이터셋
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09200008B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트