HRID1887832

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2762479

2-(Morpholin-4-yl)pyridine-4-carboxylic acid

C10H12N2O3

结构：NCc1c(-c2ncco2)n(-c2ccccc2)c2cc(Cl)ccc2c1=O

HCID71208332

未命名化合物

PRODUCTS

生成物

结构：O=C(NCc1c(-c2ncco2)n(-c2ccccc2)c2cc(Cl)ccc2c1=O)c1ccnc(N2CCOCC2)c1

HCID71208898

未命名化合物

PROCEDURE

实验过程

N-(7-Chloro-2-oxazol-2-yl-4-oxo-1-phenyl-1,4-dihydro-quinolin-3-ylmethyl)-2-morpholin-4-yl-isonicotinamide was prepared starting from intermediate A and 2-morpholinoisonicotinic acid. MS calcd. for C29H25ClN5O4 [(M+H)+] 542.2, obsd. 542.2.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-8395b00111c041749fd1fb794bb85207
来源数据集: uspto-grants-2013_08
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08501732B2
来源说明: uspto-grants-2013_08

反应 SMILES

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