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

Ethanol → N-(2H-1,3-Benzodioxol-5-yl)-6-fluoro-3-nitropyridin-2-amine

HRID 614356
노트
인쇄 미리보기

반응식

HRID 614356 반응식
C(O)C.F[C:5]1[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=[C:7]([F:14])[N:6]=1.C(=O)(O)[O-].[Na+].[CH2:20]1[O:29][C:28]2[CH:27]=[CH:26][C:24]([NH2:25])=[CH:23][C:22]=2[O:21]1>O>[F:14][C:7]1[N:6]=[C:5]([NH:25][C:24]2[CH:26]=[CH:27][C:28]3[O:29][CH2:20][O:21][C:22]=3[CH:23]=2)[C:10]([N+:11]([O-:13])=[O:12])=[CH:9][CH:8]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 702Ethanol2회HCID 843101,3-Benzodioxol-5-amineHCID 516892Sodium BicarbonateHCID 113895462,6-Difluoro-3-nitropyridine

생성물 1

HCID 21329326N-(2H-1,3-Benzodioxol-5-yl)-6-fluoro-3-nitropyridin-2-amine

시약·촉매·용매 1

HCID 962Water용매

실험 절차

In 75 ml. of ethanol was dissolved 3.2 g. (0.002 mole) of 2,6-difluoro-3-nitropyridine followed by 1.68 g. (0.02 mole) of sodium bicarbonate. To this stirred mixture, was added a solution of 2.74 g. (0.02 mole) of 3,4-(methylenedioxy) aniline in 50 ml. of ethanol dropwise over 45 minutes at room temperature. After one hour, 100 ml. of water was added and the deep-red crystalline solid product was collected. A small amount was crystallized from ethanol and melted at 161°-162° C.

후처리

  1. additionTo this stirred mixture, was added a solution of 2.74 g
  2. customthe deep-red crystalline solid product was collected
  3. customA small amount was crystallized from ethanol and melted at 161°-162° C.

출처 및 근거

ORD 기록
ord-9d51f497891740dba38ac9927bb91192
출처 데이터셋
uspto-grants-1979_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04144341

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트