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

Ammonia → 2-Amino-5-(4-chlorophenyl)pyridine-3-carbonitrile

HRID 1980305
노트
인쇄 미리보기

반응식

HRID 1980305 반응식
Cl[C:2]1[C:7]([C:8]#[N:9])=[CH:6][C:5]([C:10]2[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=2)=[CH:4][N:3]=1.[NH3:17]>CS(C)=O>[NH2:17][C:2]1[C:7]([C:8]#[N:9])=[CH:6][C:5]([C:10]2[CH:15]=[CH:14][C:13]([Cl:16])=[CH:12][CH:11]=2)=[CH:4][N:3]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222Ammonia2회HCID 27640422-Chloro-5-(4-chlorophenyl)nicotinonitrile

생성물 1

HCID 132426422-Amino-5-(4-chlorophenyl)pyridine-3-carbonitrile

시약·촉매·용매 1

HCID 679Dimethyl Sulfoxide용매2회

실험 절차

A solution of 2-chloro-5-(4-chlorophenyl)-3-pyridinecarbonitrile (2.0 grams) in 30 ml DMSO was heated in an oil bath at 80°-90° C. and then treated with gaseous NH3 for 21/2 hours. The reaction mixture was allowed to stand at room temperature for about 60 hours and then additional starting material (4 g) in 35 ml DMSO was added. The mixture was then treated with NH3 at 80°-90° C. for about 28 hours and poured into ice water. The tan solid precipitate which formed was filtered and used without further purification, yield 5.5 grams, m.p. 202°-204° C.

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트

후처리

  1. customThe tan solid precipitate which formed
  2. filtrationwas filtered
  3. customused without further purification, yield 5.5 grams, m.p. 202°-204° C.

출처 및 근거

ORD 기록
ord-9f15f1a1a74f49cf97dff05bffac1faf
출처 데이터셋
uspto-grants-1985_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US04508722

반응 노트

불러오는 중…