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Methanol → isopropyl 4-[1-phenyl-1H-[1,2,3]-triazol-4-yl]-1,2,3,6-tetrahydropyridine-1-carboxylate

HRID 2267171
ノート
印刷プレビュー

反応式

HRID 2267171 の反応式
[C:1]1([N:7]2[CH:11]=[C:10]([C:12]3[CH2:13][CH2:14][NH:15][CH2:16][CH:17]=3)[N:9]=[N:8]2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.Cl[C:19]([O:21][CH:22]([CH3:24])[CH3:23])=[O:20].CO>N1C=CC=CC=1.C(Cl)(Cl)Cl>[C:1]1([N:7]2[CH:11]=[C:10]([C:12]3[CH2:13][CH2:14][N:15]([C:19]([O:21][CH:22]([CH3:24])[CH3:23])=[O:20])[CH2:16][CH:17]=3)[N:9]=[N:8]2)[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 3

HCID 887MethanolHCID 7917Isopropyl chloroformateHCID 197052864-(1-Phenyl-1,2,3-triazol-4-yl)-1,2,3,6-tetrahydropyridine

生成物 1

HCID 58945848isopropyl 4-[1-phenyl-1H-[1,2,3]-triazol-4-yl]-1,2,3,6-tetrahydropyridine-1-carboxylate

試薬・触媒・溶媒 2

HCID 1049Pyridine溶媒HCID 6212
Chloroform
溶媒

実験手順

4-[1-phenyl-1H-[1,2,3]triazol-4-yl]-1,2,3,6-tetra-hydropyridine (35 mg) prepared in the above 1) was dissolved in 1 ml of pyridine and 1 ml of chloroform, 32 μl of isopropyl chloroformate was added and the mixture was stirred at room temperature for 1 hour. After an excessive reagent was decomposed by addition of methanol, the reaction solution was concentrated in vacuo and the resulting residue was separated and purified by a preparative thin-layer chromatography (chloroform/methanol 60/1) to give 47 mg of the title compound as a white solid.

後処理

  1. concentrationthe reaction solution was concentrated in vacuo
  2. customthe resulting residue was separated
  3. custompurified by a preparative thin-layer chromatography (chloroform/methanol 60/1)

出典と根拠

ORDレコード
ord-320a5c3ce54a48f29b8aed97787b4c46
出典データセット
uspto-grants-2010_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07858800B2

反応ノート

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