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

Sodium Hydroxide → 1-(4-Aminophenyl)-3-(3-pyridyl)-5-cyanopyrazole

HRID 1634094
노트
인쇄 미리보기

반응식

HRID 1634094 반응식
[C:1]([C:3]1[N:7]([C:8]2[CH:13]=[CH:12][C:11]([N+:14]([O-])=O)=[CH:10][CH:9]=2)[N:6]=[C:5]([C:17]2[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=2)[CH:4]=1)#[N:2].[OH-].[Na+]>Cl.CC(O)=O>[C:1]([C:3]1[N:7]([C:8]2[CH:9]=[CH:10][C:11]([NH2:14])=[CH:12][CH:13]=2)[N:6]=[C:5]([C:17]2[CH:18]=[N:19][CH:20]=[CH:21][CH:22]=2)[CH:4]=1)#[N:2]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 14798Sodium HydroxideHCID 186771255-Cyano-3-(3-pyridyl)-1-(4'-nitrophenyl)pyrazole

생성물 1

HCID 186771061-(4-Aminophenyl)-3-(3-pyridyl)-5-cyanopyrazole수율 99.5%

시약·촉매·용매 1

HCID 22641269Acetate-hydrochloric acid용매

실험 절차

5-Cyano-3-(3-pyridyl)-1-(4′-nitrophenyl)pyrazole (4.3 g, 15 mmol) was added to stirred slurry of SnCl2H2O (20 g, 90 mmol) in HCl/HOAc (35 mL/35 mL). A thick suspension formed and was stirred overnight. The reaction mixture was carefully basified with 50% NaOH to pH 13. The resulting solids were filtered, washed with water and dried to give the title compound (3.9 g, 99%).

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customA thick suspension formed
  2. filtrationThe resulting solids were filtered
  3. washwashed with water
  4. customdried

출처 및 근거

ORD 기록
ord-f17629c6ce9346c19c94859896cd558c
출처 데이터셋
uspto-grants-2003_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US06506747B1

반응 노트

불러오는 중…