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四氢呋喃 → 6-Cyclopentyl-5-methyl-nicotinic acid isopropyl ester

HRID 1908779
笔记
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反应方程式

HRID 1908779 反应方程式
[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]
参与物反应条件实验过程后处理来源与证据反应笔记

参与物

4

反应物 3

HCID 8028四氢呋喃HCID 312751,4-二氧六环HCID 866505246-Chloro-5-methylnicotinic acid isopropyl ester

产物 1

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

反应条件

温度
75 °C

实验过程

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.

后处理

  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

来源与证据

ORD记录
ord-e07c974fe81342679568f24358801085
来源数据集
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08598208B2

反应笔记

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本页导航参与物反应条件实验过程后处理来源与证据反应笔记