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

Ammonia → 3-(6-Amino-1,6-dihydro-pyridazin-4-yl)-N-methyl-benzamide

HRID 1097319
노트
인쇄 미리보기

반응식

HRID 1097319 반응식
Cl[CH:2]1[NH:7][N:6]=[CH:5][C:4]([C:8]2[CH:9]=[C:10]([CH:15]=[CH:16][CH:17]=2)[C:11]([NH:13][CH3:14])=[O:12])=[CH:3]1.[NH3:18]>CCO>[NH2:18][CH:2]1[NH:7][N:6]=[CH:5][C:4]([C:8]2[CH:9]=[C:10]([CH:15]=[CH:16][CH:17]=2)[C:11]([NH:13][CH3:14])=[O:12])=[CH:3]1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 594434963-(6-Chloro-1,6-dihydro-pyridazin-4-yl)-N-methyl-benzamide

생성물 1

HCID 594434953-(6-Amino-1,6-dihydro-pyridazin-4-yl)-N-methyl-benzamide

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
160 °C

실험 절차

3-(6-Chloro-1,6-dihydro-pyridazin-4-yl)-N-methyl-benzamide (1 eq, 2.46 mmol, 610 mg) is dissolved in a solution of NH3 (7N, 20 ml) in EtOH and heated at 160° C. in a sealed tube for 48 h. The solvent is then removed in vacuo. The reaction mixture is purified by flash column chromatography eluting with 8:2:0.5 DCM/MeOH/NH3 to give 3-(6-Amino-1,6-dihydro-pyridazin -4-yl)-N-methyl-benzamide as a brown solid; [M+H]+=229

후처리

  1. customThe solvent is then removed in vacuo
  2. customThe reaction mixture is purified by flash column chromatography
  3. washeluting with 8:2:0.5 DCM/MeOH/NH3

출처 및 근거

ORD 기록
ord-2051635063f043a298c5df2b80d2db69
출처 데이터셋
uspto-grants-2012_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08143253B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트