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

Water → 3-bromo-5-(3-methyl-1,2,4-oxadiazol-5-yl)Pyridine

HRID 1455641
노트
인쇄 미리보기

반응식

HRID 1455641 반응식
[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([CH:10]=1)[C:7]([OH:9])=O.C1N=CN(C(N2C=NC=C2)=O)C=1.O[N:24]=[C:25]([NH2:27])[CH3:26].O>CN(C=O)C.N1C=CC=CC=1>[Br:1][C:2]1[CH:3]=[N:4][CH:5]=[C:6]([C:7]2[O:9][N:27]=[C:25]([CH3:26])[N:24]=2)[CH:10]=1
참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트

참가 물질

7

반응물 4

HCID 962WaterHCID 30926N-HydroxyacetamidineHCID 682631,1'-CarbonyldiimidazoleHCID 887075-Bromonicotinic acid

생성물 1

HCID 529037353-bromo-5-(3-methyl-1,2,4-oxadiazol-5-yl)Pyridine

시약·촉매·용매 2

HCID 1049Pyridine용매HCID 6228Dimethylformamide용매

반응 조건

온도
20 °C

실험 절차

A mixture of 5-bromo nicotinic acid(1.0 eq.) and CDI (1.1 eq) in DMF (0.25M) was stirred at 20° C. for 5 min and then N′-hydroxy ethanimidamide (1.1 eq) in pyridine (0.6 M) was added. The reaction mixture was stirred at 110° C. for 15 h, cooled to rt and poured into water. The title compound was isolated by filtration as a solid.

후처리

  1. stirringThe reaction mixture was stirred at 110° C. for 15 h
  2. temperaturecooled to rt

출처 및 근거

ORD 기록
ord-8981e2f61e7b470ea2142b78ed53d923
출처 데이터셋
uspto-grants-2009_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07482456B2

반응 노트

불러오는 중…

이 페이지에서참가 물질반응 조건실험 절차후처리출처 및 근거반응 노트