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llms.txt · MCP 가이드개인정보처리방침 · 이용약관 · 지원v1.8.0
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Benzyl 2-(3-methyl[1,2,4]triazolo[4,3-a]pyridin-8-yl)acrylate → 2-(3-Methyl[1,2,4]triazolo[4,3-a]pyridin-8-yl)propanoic acid

HRID 1888198
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인쇄 미리보기

반응식

HRID 1888198 반응식
[CH3:1][C:2]1[N:6]2[CH:7]=[CH:8][CH:9]=[C:10]([C:11](=[CH2:22])[C:12]([O:14]CC3C=CC=CC=3)=[O:13])[C:5]2=[N:4][N:3]=1>[Pd].CO>[CH3:1][C:2]1[N:6]2[CH:7]=[CH:8][CH:9]=[C:10]([CH:11]([CH3:22])[C:12]([OH:14])=[O:13])[C:5]2=[N:4][N:3]=1
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참가 물질

4

반응물 1

HCID 66924470Benzyl 2-(3-methyl[1,2,4]triazolo[4,3-a]pyridin-8-yl)acrylate

생성물 1

HCID 579075822-(3-Methyl[1,2,4]triazolo[4,3-a]pyridin-8-yl)propanoic acid수율 77.6%

시약·촉매·용매 2

HCID 23938Palladium촉매HCID 887Methanol용매

실험 절차

To 0.040 mg (0.038 mmol) of 10% palladium on carbon was added a solution of (0.080 g, 0.27 mmol) of benzyl 2-(3-methyl[1,2,4]triazolo[4,3-a]pyridin-8-yl)acrylate prepared in Step C above in 4 mL of methanol. The resulting suspension was stirred under an atmosphere of hydrogen (1 atmosphere) for 6 h. The residue was filtered through a pad of Celite® and the pad was washed cold methanol. The combined filtrates were evaporated under reduced pressure to give yield the title compound (0.043 g, 77%). LC-MS: iniz (ES) 206 (MH)+.

후처리

  1. filtrationThe residue was filtered through a pad of Celite®
  2. washthe pad was washed cold methanol
  3. customThe combined filtrates were evaporated under reduced pressure
  4. customto give

출처 및 근거

ORD 기록
ord-b750d7b270114cdb82fef269e71314d1
출처 데이터셋
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08501786B2

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