HRID126824

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID10868

Dicyclohexylcarbodiimide

C13H22N2

HCID14855682

4-(Pyrrolidin-1-yl)butanoic acid--hydrogen chloride (1/1)

C8H16ClNO2

结构：CCCCCC(C)C(C)c1cc(O)c2c(c1)OC(C)(C)c1ccncc1-2

HCID19781402

未命名化合物

PRODUCTS

生成物

结构：CCCCCC(C)C(C)c1cc(OC(=O)CCCN2CCCC2)c2c(c1)OC(C)(C)c1ccncc1-2.Cl

HCID20287880

未命名化合物

PROCEDURE

实验过程

5,5-Dimethyl-8-(3-methyl-2-octyl)-10-[4-(pyrrolidino)butyryloxy]-5H-[1]benzopyrano[3,4-d]pyridine hydrochloride is prepared according to the method of Example 29 by reacting equimolar quantities of 5,5-dimethyl-10-hydroxy-8-(3-methyl-2-octyl)-5H-[1]benzopyrano[3,4-d]pyridine and γ-pyrrolidinobutyric acid hydrochloride in the presence of dicyclohexyl carbodiimide.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-632520cbbf3b423e9a18c86b8716fc49
来源数据集: uspto-grants-1981_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04254116
来源说明: uspto-grants-1981_03

反应 SMILES

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