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Methanol → HCID 25255501,化合物

HRID 74331
笔记
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反应方程式

HRID 74331 反应方程式
[CH:1]1([CH2:8][O:9][C:10]2[CH:11]=[C:12]([CH2:16][CH2:17][CH2:18][NH:19]C(=O)C(F)(F)F)[CH:13]=[CH:14][CH:15]=2)[CH2:7][CH2:6][CH2:5][CH2:4][CH2:3][CH2:2]1.CO>O>[CH:1]1([CH2:8][O:9][C:10]2[CH:11]=[C:12]([CH2:16][CH2:17][CH2:18][NH2:19])[CH:13]=[CH:14][CH:15]=2)[CH2:2][CH2:3][CH2:4][CH2:5][CH2:6][CH2:7]1
参与物实验过程后处理来源与证据反应笔记

参与物

4

反应物 2

HCID 887MethanolHCID 86637612N-(3-(3-(cycloheptylmethoxy)phenyl)propyl)-2,2,2-trifluoroacetamide

产物 1

HCID 25255501HCID 25255501,化合物

试剂、催化剂与溶剂 1

HCID 962聚[6-[4-(4-氰基苯基)苯氧基]己基甲基丙烯酸酯]溶剂

实验过程

N-(3-(3-(cycloheptylmethoxy)phenyl)propyl)-2,2,2-trifluoroacetamide was deprotected following the method used in Example 10 except that the MeOH:water mixture was 4:1. After the extractive work up, the residue was dissolved in hexanes, filtered through Celite and concentrated under reduced pressure. Example 14 was isolated in pure form without further manipulation. 1H NMR (400 MHz, CDCl3) δ 7.17 (t, J=7.6 Hz, 1H), 6.70-6.76 (m, 3H), 3.71 (d, J=6.8 Hz, 2H), 2.74 (t, J=7.2 Hz, 2H), 2.62 (t, J=8 Hz, 2H), 1.43-2.02 (m, 15H), 1.23-1.33 (m, 2H).

后处理

  1. filtrationfiltered through Celite
  2. concentrationconcentrated under reduced pressure
  3. customExample 14 was isolated in pure form without further manipulation

来源与证据

ORD记录
ord-0edb9fd0e5514bea89a4c1b94bbb2d22
来源数据集
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08829244B2

反应笔记

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本页导航参与物实验过程后处理来源与证据反应笔记