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

Ammonia → 6-Chloro-5-(2-chloro-5-methoxy-phenoxy)-pyrimidin-4-ylamine

HRID 356648
노트
인쇄 미리보기

반응식

HRID 356648 반응식
[NH3:1].[Cl:2][C:3]1[C:8]([O:9][C:10]2[CH:15]=[C:14]([O:16][CH3:17])[CH:13]=[CH:12][C:11]=2[Cl:18])=[C:7](Cl)[N:6]=[CH:5][N:4]=1>C(O)C>[Cl:2][C:3]1[N:4]=[CH:5][N:6]=[C:7]([NH2:1])[C:8]=1[O:9][C:10]1[CH:15]=[C:14]([O:16][CH3:17])[CH:13]=[CH:12][C:11]=1[Cl:18]
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 2

HCID 222AmmoniaHCID 219795664,6-Dichloro-5-(2-chloro-5-methoxy-phenoxy)-pyrimidine

생성물 1

HCID 189389356-Chloro-5-(2-chloro-5-methoxy-phenoxy)-pyrimidin-4-ylamine

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
-78 °C

실험 절차

About 500 ml of NH3 were conducted at -78° C. into a solution of 9.9 g of 4,6-dichloro-5-(2-chloro-5-methoxy-phenoxy)-pyrimidine from Example 1e) in 400 ml of ethanol. Thereafter, the reaction mixture was stirred at -78° C. for 15 hours and at room temperature for 50 hours and finally evaporated. The residue was partitioned between ethyl acetate and water and the organic phase was worked-up. 8.53 g of 6-chloro-5-(2-chloro-5-methoxy-phenoxy)-pyrimidin-4-ylamine were thus obtained as yellow crystals. MS: 285 (M).

후처리

  1. customfinally evaporated
  2. customThe residue was partitioned between ethyl acetate and water

출처 및 근거

ORD 기록
ord-252be7112c9a4953a96efe6692e43e3a
출처 데이터셋
uspto-grants-1998_11
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05837708

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트