HRID38462

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：Cl.Cn1cc(-c2ccc3c(c2)C(=O)CC2(CCNCC2)O3)cn1

HCID66782546

未命名化合物

结构：CCOc1cc(C(=O)O)cc(OCC)c1-c1ccc(C(=O)OC)cc1

HCID67055548

未命名化合物

PRODUCTS

生成物

结构：CCOc1cc(C(=O)N2CCC3(CC2)CC(=O)c2cc(-c4cnn(C)c4)ccc2O3)cc(OCC)c1-c1ccc(C(=O)OC)cc1

HCID58208685

未命名化合物

PROCEDURE

实验过程

In the same manner as in Example 25, the intended compound was obtained as a colorless solid using 6-(1-methyl-1H-pyrazol-4-yl)spiro[chroman-2,4′-piperidin]-4-one hydrochloride and 2,6-diethoxy-4′-(methoxycarbonyl)biphenyl-4-carboxylic acid.

WORKUP

后处理

customIn the same manner as in Example 25, the intended compound was obtained as a colorless solid

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-2b7a8ebb808649f2bc3efd76d413ddec
来源数据集: uspto-grants-2013_09
DOI: 10.6084/m9.figshare.5104873.v1
专利: US08524730B2
来源说明: uspto-grants-2013_09

反应 SMILES

Cl.[CH3:2][N:3]1[CH:7]=[C:6]([C:8]2[CH:9]=[C:10]3[C:20](=[CH:21][CH:22]=2)[O:19][C:13]2([CH2:18][CH2:17][NH:16][CH2:15][CH2:14]2)[CH2:12][C:11]3=[O:23])[CH:5]=[N:4]1.[CH2:24]([O:26][C:27]1[CH:32]=[C:31]([C:33](O)=[O:34])[CH:30]=[C:29]([O:36][CH2:37][CH3:38])[C:28]=1[C:39]1[CH:44]=[CH:43][C:42]([C:45]([O:47][CH3:48])=[O:46])=[CH:41][CH:40]=1)[CH3:25]>>[CH2:37]([O:36][C:29]1[CH:30]=[C:31]([C:33]([N:16]2[CH2:15][CH2:14][C:13]3([CH2:12][C:11](=[O:23])[C:10]4[C:20](=[CH:21][CH:22]=[C:8]([C:6]5[CH:5]=[N:4][N:3]([CH3:2])[CH:7]=5)[CH:9]=4)[O:19]3)[CH2:18][CH2:17]2)=[O:34])[CH:32]=[C:27]([O:26][CH2:24][CH3:25])[C:28]=1[C:39]1[CH:40]=[CH:41][C:42]([C:45]([O:47][CH3:48])=[O:46])=[CH:43][CH:44]=1)[CH3:38]