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llms.txt · MCPガイドプライバシーポリシー · 利用規約 · サポートv1.8.0
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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
ノート
印刷プレビュー

反応式

HRID 1888198 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

4

反応物 1

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 23938Palladium触媒HCID 887Methanol溶媒

実験手順

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)+.

後処理

  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

出典と根拠

ORDレコード
ord-b750d7b270114cdb82fef269e71314d1
出典データセット
uspto-grants-2013_08
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08501786B2

反応ノート

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