HRID427101

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID10868

Dicyclohexylcarbodiimide

C13H22N2

HCID12691640

4-(Dimethylamino)butanoic acid--hydrogen chloride (1/1)

C6H14ClNO2

结构：CCCCCC(C)C(C)c1cc(O)c2c(c1)OC(C)(C)C1=C2CN(CC(=O)NC(N)=O)CC1

HCID20388001

未命名化合物

PRODUCTS

生成物

结构：CCCCCC(C)C(C)c1cc(OC(=O)CCCN(C)C)c2c(c1)OC(C)(C)C1=C2CN(CC(=O)NC(N)=O)CC1.Cl

HCID86736689

未命名化合物

PROCEDURE

实验过程

The above-titled compound was prepared according to the method of Example 8 by reacting equimolar quantities of {[10-hydroxy-5,5-dimethyl-8-(1,2-dimethylheptyl)-1,2,3,4-tetrahydro-5H-[1]benzopyrano[4,3-c]pyridin-2-yl]acetyl}urea and 4-(dimethylamino)butyric acid hydrochloride in the presence of dicyclohexylcarbodiimide.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-0f5e09675d83427d9ad4635a47bd9a40
来源数据集: uspto-grants-1979_10
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04172943
来源说明: uspto-grants-1979_10

反应 SMILES

[OH:1][C:2]1[C:7]2[C:8]3[CH2:9][N:10]([CH2:18][C:19]([NH:21][C:22]([NH2:24])=[O:23])=[O:20])[CH2:11][CH2:12][C:13]=3[C:14]([CH3:17])([CH3:16])[O:15][C:6]=2[CH:5]=[C:4]([CH:25]([CH3:33])[CH:26]([CH3:32])[CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])[CH:3]=1.[ClH:34].[CH3:35][N:36]([CH3:43])[CH2:37][CH2:38][CH2:39][C:40](O)=[O:41].C1(N=C=NC2CCCCC2)CCCCC1>>[ClH:34].[CH3:17][C:14]1([CH3:16])[C:13]2[CH2:12][CH2:11][N:10]([CH2:18][C:19]([NH:21][C:22]([NH2:24])=[O:23])=[O:20])[CH2:9][C:8]=2[C:7]2[C:2]([O:1][C:40](=[O:41])[CH2:39][CH2:38][CH2:37][N:36]([CH3:43])[CH3:35])=[CH:3][C:4]([CH:25]([CH3:33])[CH:26]([CH3:32])[CH2:27][CH2:28][CH2:29][CH2:30][CH3:31])=[CH:5][C:6]=2[O:15]1