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

Ethylamine → N-(2,6-Dichloro-3-pyridinyl)-2-ethylamino-3-pyridinecarboxamide

HRID 724932
노트
인쇄 미리보기

반응식

HRID 724932 반응식
[Cl:1][C:2]1[C:7]([NH:8][C:9]([C:11]2[C:12](Cl)=[N:13][CH:14]=[CH:15][CH:16]=2)=[O:10])=[CH:6][CH:5]=[C:4]([Cl:18])[N:3]=1.[CH2:19]([NH2:21])[CH3:20]>>[Cl:1][C:2]1[C:7]([NH:8][C:9]([C:11]2[C:12]([NH:21][CH2:19][CH3:20])=[N:13][CH:14]=[CH:15][CH:16]=2)=[O:10])=[CH:6][CH:5]=[C:4]([Cl:18])[N:3]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 6341EthylamineHCID 10447677HCID 10447677, 화합물

생성물 1

HCID 10828808N-(2,6-Dichloro-3-pyridinyl)-2-ethylamino-3-pyridinecarboxamide수율 59.8%

반응 조건

온도
165 °C

실험 절차

A mixture of N-(2,6-dichloro-3-pyridinyl)-2-chloro-3-pyridinecarboxamide (12.0 g, 39.8 mmol), ethylamine (3.6 g, 80.7 mmol), and 30 mL of xylenes in a sealed vessel was heated at 165° C. for 6 hours. The reaction mixture was cooled to room temperature and extracted with ethyl acetate to give 7.4 g of the title compound, suitable for use in the next reaction.

후처리

  1. temperatureThe reaction mixture was cooled to room temperature
  2. extractionextracted with ethyl acetate
이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

출처 및 근거

ORD 기록
ord-d811efcc7f87451b9de09fc8bed1e8c3
출처 데이터셋
uspto-grants-1998_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05705499

반응 노트

불러오는 중…