HRID352750

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID1512540

未命名化合物

结构：Cl.O=S(=O)(c1ccc2cc(Cl)ccc2c1)N1CCNCC1

HCID22709766

未命名化合物

PRODUCTS

生成物

结构：CC(C)(C)OC(=O)N1CCC(CCC(=O)N2CCN(S(=O)(=O)c3ccc4cc(Cl)ccc4c3)CC2)CC1

HCID22709824

未命名化合物

PROCEDURE

实验过程

In the same manner as in Referential Example 12, a reaction was conducted using 3-(1-tert-butoxycarbonylpiperidin-4-yl)propionic acid and 1-[(6-chloronaphthalen-2-yl)sulfonyl]-piperazine hydrochloride as starting materials, whereby the title compound was obtained.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-95b465cafd4a40f2a21f4124ec1f2a65
来源数据集: uspto-grants-2004_06
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06747023B1
来源说明: uspto-grants-2004_06

反应 SMILES

[C:1]([O:5][C:6]([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][CH2:15][C:16]([OH:18])=O)[CH2:10][CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].Cl.[Cl:20][C:21]1[CH:22]=[C:23]2[C:28](=[CH:29][CH:30]=1)[CH:27]=[C:26]([S:31]([N:34]1[CH2:39][CH2:38][NH:37][CH2:36][CH2:35]1)(=[O:33])=[O:32])[CH:25]=[CH:24]2>>[C:1]([O:5][C:6]([N:8]1[CH2:9][CH2:10][CH:11]([CH2:14][CH2:15][C:16]([N:37]2[CH2:36][CH2:35][N:34]([S:31]([C:26]3[CH:25]=[CH:24][C:23]4[C:28](=[CH:29][CH:30]=[C:21]([Cl:20])[CH:22]=4)[CH:27]=3)(=[O:33])=[O:32])[CH2:39][CH2:38]2)=[O:18])[CH2:12][CH2:13]1)=[O:7])([CH3:2])([CH3:3])[CH3:4]