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Tetrahydrofuran → 6-Cyclopentyl-5-methyl-nicotinic acid isopropyl ester

HRID 1908779
ノート
印刷プレビュー

反応式

HRID 1908779 の反応式
[CH:1]([O:4][C:5](=[O:14])[C:6]1[CH:11]=[C:10]([CH3:12])[C:9](Cl)=[N:8][CH:7]=1)([CH3:3])[CH3:2].[CH2:15]1[CH2:19]O[CH2:17][CH2:16]1.O1CCOC[CH2:21]1>>[CH:1]([O:4][C:5](=[O:14])[C:6]1[CH:11]=[C:10]([CH3:12])[C:9]([CH:15]2[CH2:19][CH2:21][CH2:17][CH2:16]2)=[N:8][CH:7]=1)([CH3:3])[CH3:2]
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

4

反応物 3

HCID 8028TetrahydrofuranHCID 312751,4-DioxaneHCID 866505246-Chloro-5-methylnicotinic acid isopropyl ester

生成物 1

HCID 670269086-Cyclopentyl-5-methyl-nicotinic acid isopropyl ester

反応条件

温度
75 °C

実験手順

Under argon, Pd(dppf) (11 mg, 14 μmol) is added to a solution of 6-chloro-5-methyl-nicotinic acid isopropyl ester (300 mg, 1.40 mmol) in dioxane (60 mL). To this mixture, a 0.5 M solution of cyclopentyl zink chloride in THF (452 mg, 2.11 mmol, 4.2 mL) is added dropwise. The mixture is stirred at 75° C. for 18 h before it is cooled to rt and quenched with water. The mixture is further diluted with water and extracted twice with EA (100 mL). The combined org. extracts are dried over MgSO4, filtered and concentrated. The crude product is purified on prep. TLC plates with heptane:EA 1:1 to give 6-cyclopentyl-5-methyl-nicotinic acid isopropyl ester (138 mg) as a pale yellow oil; LC-MS: tR=0.91 min; [M+1]+=248.53.

後処理

  1. temperatureis cooled to rt
  2. customquenched with water
  3. additionThe mixture is further diluted with water
  4. extractionextracted twice with EA (100 mL)
  5. dry with materialextracts are dried over MgSO4
  6. filtrationfiltered
  7. concentrationconcentrated
  8. customThe crude product is purified on prep

出典と根拠

ORDレコード
ord-e07c974fe81342679568f24358801085
出典データセット
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08598208B2

反応ノート

読み込み中…

このページの内容参加物反応条件実験手順後処理出典と根拠反応ノート