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

Methylamine → 4-Methylamino-[1,2,4]triazolo[4,3-a]quinoxaline

HRID 464284
노트
인쇄 미리보기

반응식

HRID 464284 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][NH2:16]>CN(C)C=O>[CH3:15][NH:16][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 6329MethylamineHCID 11261184-Chloro[1,2,4]triazolo[4,3-a]quinoxaline

생성물 1

HCID 133856804-Methylamino-[1,2,4]triazolo[4,3-a]quinoxaline수율 69%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

4-Chloro-[1,2,4]triazolo-[4,3-a]quinoxaline (2.0 g., 0.01 mole), the product of Example 2, in N,N-dimethyl formamide (30 ml.) was saturated with monomethylamine gas and stirred at room temperature for 3 hours. Monomethylamine gas was again bubbled into the solution and the solution was stirred at room temperature for an additional 2 hours. The precipitate was separated by filtration and washed with N,N-dimethylformamide. Recrystallization from N,N-dimethylformamide gave 1.37 g. (69% yield) of 4-methylamino-[1,2,4]triazolo[4,3-a]quinoxaline, m.p. >300° C. Mass spectrum: m/e, 199 (P).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customMonomethylamine gas was again bubbled into the solution
  2. stirringthe solution was stirred at room temperature for an additional 2 hours
  3. customThe precipitate was separated by filtration
  4. washwashed with N,N-dimethylformamide
  5. customRecrystallization from N,N-dimethylformamide
  6. customgave 1.37 g

출처 및 근거

ORD 기록
ord-2dff22469f354642a4f50a84a904df53
출처 데이터셋
uspto-grants-1985_10
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04547501

반응 노트

불러오는 중…