HRID625338

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID168937

Lithium hydroxide, monohydrate

H3LiO2

结构：COC(=O)c1ccnc(-c2cc(N3CCCCC3)ccc2NC(=O)c2cccc(C(=O)N(C)CCN3CCOCC3)c2)c1

HCID66588050

未命名化合物

PRODUCTS

生成物

结构：CN(CCN1CCOCC1)C(=O)c1cccc(C(=O)Nc2ccc(N3CCCCC3)cc2-c2cc(C(=O)O)ccn2)c1

HCID66588049

未命名化合物

收率 124.2%

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID21886435

1,4-Dioxane--water (1/1)

C4H10O3

PROCEDURE

实验过程

A solution of 231 mg of methyl 2-(2-(3-(methyl(2-morpholinoethyl)carbamoyl)benzamido)-5-(piperidin-1-yl)phenyl)isonicotinate in 9 mL of 2:1 dioxane/water was treated with 33 mg of lithium hydroxide hydrate. After stirring for 1 h the solvent was evaporated and the residue was partitioned between dichloromethane and 3 N hydrochloric acid. The aqueous phase was evaporated to give the product as 280 mg of a yellow solid.

WORKUP

后处理

customwas evaporated
customthe residue was partitioned between dichloromethane and 3 N hydrochloric acid
customThe aqueous phase was evaporated

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-e104531fd18845f69cbb097a9f1d5cd5
来源数据集: uspto-grants-2016_04
DOI: 10.6084/m9.figshare.5104873.v1
专利: US09301951B2
来源说明: uspto-grants-2016_04

反应 SMILES

[CH3:1][N:2]([CH2:36][CH2:37][N:38]1[CH2:43][CH2:42][O:41][CH2:40][CH2:39]1)[C:3]([C:5]1[CH:6]=[C:7]([CH:33]=[CH:34][CH:35]=1)[C:8]([NH:10][C:11]1[CH:16]=[CH:15][C:14]([N:17]2[CH2:22][CH2:21][CH2:20][CH2:19][CH2:18]2)=[CH:13][C:12]=1[C:23]1[CH:24]=[C:25]([CH:30]=[CH:31][N:32]=1)[C:26]([O:28]C)=[O:27])=[O:9])=[O:4].O.[OH-].[Li+]>O1CCOCC1.O>[CH3:1][N:2]([CH2:36][CH2:37][N:38]1[CH2:39][CH2:40][O:41][CH2:42][CH2:43]1)[C:3]([C:5]1[CH:6]=[C:7]([CH:33]=[CH:34][CH:35]=1)[C:8]([NH:10][C:11]1[CH:16]=[CH:15][C:14]([N:17]2[CH2:18][CH2:19][CH2:20][CH2:21][CH2:22]2)=[CH:13][C:12]=1[C:23]1[CH:24]=[C:25]([CH:30]=[CH:31][N:32]=1)[C:26]([OH:28])=[O:27])=[O:9])=[O:4]