HRID1434851

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID5237175

tert-Butyl 3-(hydroxymethyl)pyrrolidine-1-carboxylate

C10H19NO3

结构：Cc1ccc(C(=S)Nc2cccnc2C(=O)Nc2ccc(Cl)cn2)c(O)c1

HCID136348818

未命名化合物

PRODUCTS

生成物

结构：Cc1ccc(C(=S)Nc2cccnc2C(=O)Nc2ccc(Cl)cn2)c(OCC2CCN(C(=O)OC(C)(C)C)C2)c1

HCID86620007

未命名化合物

PROCEDURE

实验过程

Using a procedure analogous to Example 38-D, 1-t-butoxycarbonylpyrrolidine-3-methanol (Isomer I) and N-(5-chloropyridin-2-yl)-3-[2-hydroxy-4-methylthiobenzoyl-amino]pyridine-2-carboxamide gave the title compound as a solid (1.7 g).

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-b3c4c2e3b5ec4db4aa5f06e51f43b5b2
来源数据集: uspto-grants-2009_11
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07615568B2
来源说明: uspto-grants-2009_11

反应 SMILES

[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH:10]([CH2:13][OH:14])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2].[Cl:15][C:16]1[CH:17]=[CH:18][C:19]([NH:22][C:23]([C:25]2[C:30]([NH:31][C:32](=[S:41])[C:33]3[CH:38]=[CH:37][C:36]([CH3:39])=[CH:35][C:34]=3O)=[CH:29][CH:28]=[CH:27][N:26]=2)=[O:24])=[N:20][CH:21]=1>>[C:1]([O:5][C:6]([N:8]1[CH2:12][CH2:11][CH:10]([CH2:13][O:14][C:34]2[CH:35]=[C:36]([CH3:39])[CH:37]=[CH:38][C:33]=2[C:32]([NH:31][C:30]2[C:25]([C:23]([NH:22][C:19]3[CH:18]=[CH:17][C:16]([Cl:15])=[CH:21][N:20]=3)=[O:24])=[N:26][CH:27]=[CH:28][CH:29]=2)=[S:41])[CH2:9]1)=[O:7])([CH3:4])([CH3:3])[CH3:2]