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

[1,2,4]Triazolo[1,5-a]pyridin-2-ylmethanol → HCID 72207223, 화합물

HRID 1615625
노트
인쇄 미리보기

반응식

HRID 1615625 반응식
[N:1]1[C:2]([CH2:10][OH:11])=[N:3][N:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=12>CCO.[O-2].[Mn+4].[O-2]>[N:1]1[C:2]([CH:10]=[O:11])=[N:3][N:4]2[CH:9]=[CH:8][CH:7]=[CH:6][C:5]=12
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

4

반응물 1

HCID 18406865[1,2,4]Triazolo[1,5-a]pyridin-2-ylmethanol

생성물 1

HCID 72207223HCID 72207223, 화합물수율 44.3%

시약·촉매·용매 2

HCID 178418406HCID 178418406, 화합물촉매HCID 702Ethanol용매

실험 절차

To a solution of [1,2,4]triazolo[1,5-a]pyridin-2-ylmethanol (0.35 g, 2.3 mmol) in EtOH (50 mL) was added manganese (IV) oxide (1.02 g, 11.5 mmol). The mixture was refluxed for 2 days. After cooling to room temperature, the mixture was filtered through Celite. The filtrate was concentrated, and the residue was purified by reverse phase column chromatography (eluting with 10% v/v acetonitrile in water, with 0.01% NH3.H2O) to afford the title compound (0.15 g, 43% yield) as a white solid. ESI MS: m/z 148 [M+H]+.

후처리

  1. temperatureThe mixture was refluxed for 2 days
  2. filtrationthe mixture was filtered through Celite
  3. concentrationThe filtrate was concentrated
  4. customthe residue was purified by reverse phase column chromatography (
  5. washeluting with 10% v/v acetonitrile in water, with 0.01% NH3.H2O)

출처 및 근거

ORD 기록
ord-770550ffb68f4471a8d3f521eff936c9
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08765760B2

반응 노트

불러오는 중…

이 페이지에서참가 물질실험 절차후처리출처 및 근거반응 노트