HRID1864371

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2760057

1-(3-Methylpyridin-2-yl)piperazine

C10H15N3

结构：COc1cccc(S(=O)(=O)N2CC(C(=O)O)N(c3ccccc3)C2=O)c1

HCID67141122

未命名化合物

PRODUCTS

生成物

结构：COc1cccc(S(=O)(=O)N2CC(C(=O)N3CCN(c4ncccc4C)CC3)N(c3ccccc3)C2=O)c1

HCID25027712

未命名化合物

PROCEDURE

实验过程

In analogy to example 1, (RS)-1-(3-methoxy-benzenesulfonyl)-2-oxo-3-phenyl-imidazolidine-4-carboxylic acid (step 4 of example 1) was reacted with 1-(3-methyl-pyridin-2-yl)piperazine to give the title compound as a colorless solid. MS: 536.2 ([M+H]+)

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-cbe2070fa3a046b9b93d819c42332c47
来源数据集: uspto-grants-2009_12
DOI: 10.6084/m9.figshare.5104873.v1
专利: US07625902B2
来源说明: uspto-grants-2009_12

反应 SMILES

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