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

2-Amino-2-methyl-1,3-propanediol → [2-(6-Chloropyridin-3-yl)-4-methyl-4,5-dihydro-1,3-oxazol-4-yl]methanol

HRID 251455
노트
인쇄 미리보기

반응식

HRID 251455 반응식
[Cl:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([OH:8])=O)=[CH:4][N:3]=1.[NH2:11][C:12]([CH3:17])([CH2:15]O)[CH2:13][OH:14]>>[Cl:1][C:2]1[N:3]=[CH:4][C:5]([C:6]2[O:8][CH2:15][C:12]([CH2:13][OH:14])([CH3:17])[N:11]=2)=[CH:9][CH:10]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

3

반응물 2

HCID 15312-Amino-2-methyl-1,3-propanediolHCID 792226-Chloronicotinic acid

생성물 1

HCID 11950723[2-(6-Chloropyridin-3-yl)-4-methyl-4,5-dihydro-1,3-oxazol-4-yl]methanol수율 40%

실험 절차

A suspension of 6-chloronicotinic acid (3.2 g, 20.4 mmol) and 2-amino-2-methyl-1,3-propanediol (2.1 g, 20 mmol) in xylenes (mixture of isomers, 80 ml) is heated at reflux under Dean-Stark conditions for 24 h, during which the mixture clarifies. Upon cooling to room temperature, a solid settles down. The mixture is filtered through a silicagel column, eluting first with hexane to remove the xylenes and then with ethyl acetate to afford 1.8 g of [2-(6-chloropyridin-3-yl)-4-methyl-4,5-dihydro-1,3-oxazol-4-yl]methanol ax55.

후처리

  1. temperatureis heated
  2. temperatureat reflux under Dean-Stark conditions for 24 h, during which the mixture
이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트
filtration
The mixture is filtered through a silicagel column
  • washeluting first with hexane
  • customto remove the xylenes
  • 출처 및 근거

    ORD 기록
    ord-3ed7faf4dcc744dea7987ccf4aab5613
    출처 데이터셋
    uspto-grants-2011_01
    DOI
    10.6084/m9.figshare.5104873.v1
    특허 번호
    US07863450B2

    반응 노트

    불러오는 중…