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

Dimethylamine → 4-Dimethylamino-[1,2,4]triazolo[4,3-a]quinoxaline

HRID 464285
노트
인쇄 미리보기

반응식

HRID 464285 반응식
Cl[C:2]1[C:3]2[N:4]([CH:12]=[N:13][N:14]=2)[C:5]2[C:10]([N:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2.[CH3:15][NH:16][CH3:17]>CN(C)C=O>[CH3:15][N:16]([CH3:17])[C:2]1[C:3]2[N:4]([CH:12]=[N:13][N:14]=2)[C:5]2[C:10]([N:11]=1)=[CH:9][CH:8]=[CH:7][CH:6]=2
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 674DimethylamineHCID 11261184-Chloro[1,2,4]triazolo[4,3-a]quinoxaline

생성물 1

HCID 66229934-Dimethylamino-[1,2,4]triazolo[4,3-a]quinoxaline수율 44%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

A slurry of 2.0 g. (0.01 mole) of 4-chloro-[1,2,4]triazolo[4,3-a]quinoxaline (the product of Example 2) in N,N-dimethylformamide (30 ml.) was saturated with dimethylamine gas and stirred at room temperature overnight. The mixture was poured over ice and the precipitate was removed by filtration. Recrystallization from ethanol gave 640 mg. (44% yield) of 4-dimethylamino-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. 184°-186° C. Mass spectrum: m/e, 213 (P).

후처리

  1. additionThe mixture was poured over ice
  2. customthe precipitate was removed by filtration
  3. customRecrystallization from ethanol
  4. customgave 640 mg

출처 및 근거

ORD 기록
ord-9b54e143db7f48f399a73e6fb77c3b07
출처 데이터셋
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04547501

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트