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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Methanol, 1,1-diethoxy-, 1-acetate → 5-Bromo-(1,2,4)triazolo(4,3-a)pyridine

HRID 1945600
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반응식

HRID 1945600 반응식
[Br:1][C:2]1[N:7]=[C:6]([NH:8][NH2:9])[CH:5]=[CH:4][CH:3]=1.[C:10](OC(OCC)OCC)(=O)C>CCCCC>[Br:1][C:2]1[N:7]2[CH:10]=[N:9][N:8]=[C:6]2[CH:5]=[CH:4][CH:3]=1
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참가 물질

4

반응물 2

HCID 84166Methanol, 1,1-diethoxy-, 1-acetateHCID 193925882-Bromo-6-hydrazinopyridine

생성물 1

HCID 441183095-Bromo-(1,2,4)triazolo(4,3-a)pyridine수율 78%

시약·촉매·용매 1

HCID 8003Pentane용매

실험 절차

A solution of (6-bromopyridin-2-yl)hydrazine (500 mg, 2.66 mmol) in diethoxymethyl acetate (2.5 mL) was stirred at room temperature for 18 hours. The reaction mixture was diluted with pentane and filtered. The precipitate was washed with pentane and dried at 50° C. under vacuum for 1 hour to give 5-bromo-[1,2,4]triazolo[4,3-a]pyridine as a beige solid (410 mg, 78%). 1H NMR (400 MHz, CHCl3-d): δ 8.98 (s, 1 H); 7.83 (dt, J=9.2, 0.9 Hz, 1 H); 7.22 (dd, J=9.2, 7.0 Hz, 1 H); 7.09 (dd, J=7.0, 0.9 Hz, 1 H).

후처리

  1. filtrationfiltered
  2. washThe precipitate was washed with pentane
  3. customdried at 50° C. under vacuum for 1 hour

출처 및 근거

ORD 기록
ord-f045edc9168a4d579f5e77feb4960888
출처 데이터셋
uspto-grants-2013_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08394796B2

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