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氯甲酸甲酯 → (R) - (3-氯苯基)(2 - ((甲氧羰基)氨基)乙氧基)甲基)哌啶-1-甲酸叔丁酯

HRID 451663
笔记
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反应方程式

HRID 451663 反应方程式
[NH2:1][CH2:2][CH2:3][O:4][C@@H:5]([C:19]1[CH:24]=[CH:23][CH:22]=[C:21]([Cl:25])[CH:20]=1)[C@@H:6]1[CH2:11][CH2:10][CH2:9][N:8]([C:12]([O:14][C:15]([CH3:18])([CH3:17])[CH3:16])=[O:13])[CH2:7]1.CCN(CC)CC.Cl[C:34]([O:36][CH3:37])=[O:35]>CN(C1C=CN=CC=1)C.C(Cl)Cl>[Cl:25][C:21]1[CH:20]=[C:19]([C@H:5]([O:4][CH2:3][CH2:2][NH:1][C:34]([O:36][CH3:37])=[O:35])[C@@H:6]2[CH2:11][CH2:10][CH2:9][N:8]([C:12]([O:14][C:15]([CH3:18])([CH3:16])[CH3:17])=[O:13])[CH2:7]2)[CH:24]=[CH:23][CH:22]=1
参与物实验过程后处理来源与证据反应笔记

参与物

6

反应物 3

HCID 6586氯甲酸甲酯HCID 8471三乙胺HCID 59598469(R)-tert-butyl 3-((R)-(2-aminoethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate

产物 1

HCID 59598498(R) - (3-氯苯基)(2 - ((甲氧羰基)氨基)乙氧基)甲基)哌啶-1-甲酸叔丁酯收率 58.6%

试剂、催化剂与溶剂 2

HCID 142844-二甲氨基吡啶(DMAP)催化剂
HCID 6344
二氯甲烷
溶剂
2 次

实验过程

To a solution of (R)-tert-butyl 3-((R)-(2-aminoethoxy)(3-chlorophenyl)methyl)piperidine-1-carboxylate (1.05 g, ca. 2.6 mmol), Et3N (3.96 mL, 2.85 mmol), and DMAP (174 mg, 1.43 mmol) in anhydrous CH2Cl2 (20 mL) cooled to 0° C. was added a solution of methyl chloroformate (1.35 g, 14.25 mmol) in dichloromethane (20 mL) within 30 min. The reaction was stirred overnight, and evaporated under vacuum. The residue was purified by flash chromatography on silica gel to afford (R)-tert-butyl 3-((R)-(3-chlorophenyl)(2-(methoxycarbonylamino)ethoxy)methyl)piperidine-1-carboxylate (0.65 g). MS: 427 (M+H)+.

后处理

  1. customevaporated under vacuum
  2. customThe residue was purified by flash chromatography on silica gel

来源与证据

ORD记录
ord-268a0240bc19487294c1a896f2ade3b3
来源数据集
uspto-grants-2013_07
DOI
10.6084/m9.figshare.5104873.v1
专利号
US08487108B2

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