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4-氮杂卓醇 → Methyl 4-bromo-3-(4-hydroxyazepan-1-yl)sulfonyl-benzoate

HRID 1754300
笔记
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反应方程式

HRID 1754300 反应方程式
[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][C:3]=1[S:12](Cl)(=[O:14])=[O:13].[NH:16]1[CH2:22][CH2:21][CH2:20][CH:19]([OH:23])[CH2:18][CH2:17]1>C(Cl)Cl>[Br:1][C:2]1[CH:11]=[CH:10][C:5]([C:6]([O:8][CH3:9])=[O:7])=[CH:4][C:3]=1[S:12]([N:16]1[CH2:22][CH2:21][CH2:20][CH:19]([OH:23])[CH2:18][CH2:17]1)(=[O:14])=[O:13]
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 2

HCID 51497464-氮杂卓醇HCID 194291974-溴-3-(氯磺酰基)苯甲酸甲酯

产物 1

HCID 118222058Methyl 4-bromo-3-(4-hydroxyazepan-1-yl)sulfonyl-benzoate收率 77.5%

试剂、催化剂与溶剂 1

HCID 6344二氯甲烷溶剂

反应条件

温度
25 °C

实验过程

To a solution of methyl 4-bromo-3-chlorosulfonyl-benzoate (7.22 g, 23.03 mmol, 1.00 Eq) in DCM (100 mL) was added azepan-4-ol (2.65 g, 23.03 mmol, 1.00 Eq) and TEA (2.33 g, 23.03 mmol, 1.00 Eq). The resulting mixture was stirred at 25° C. until the starting material was consumed. The solvent was removed and the residue was purified by silica gel chromatography (PE:EA=1:1) to give desired compound methyl 4-bromo-3-(4-hydroxyazepan-1-yl)sulfonyl-benzoate (7.00 g, 17.85 mmol, 77.49% yield). LCMS: 393/395 [M+1].

后处理

  1. customwas consumed
  2. customThe solvent was removed
  3. customthe residue was purified by silica gel chromatography (PE:EA=1:1)

来源与证据

ORD记录
ord-131c3ad461b842a69d21fcb47ddda90b
来源数据集
uspto-grants-2015_10
DOI
10.6084/m9.figshare.5104873.v1
专利号
US09169212B2

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