HRID1872075

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID10657952

未命名化合物

结构：Cc1nnc(-c2ccc(-c3ccc(C(=O)O)cc3)c(C)c2)o1

HCID18690066

未命名化合物

PRODUCTS

生成物

结构：Cc1nnc(-c2ccc(-c3ccc(C(=O)N4CCc5cc6c(cc54)C4(CCN(C)CC4)CO6)cc3)c(C)c2)o1

HCID9892896

未命名化合物

PROCEDURE

实验过程

The title compound was prepared from 1'-methyl-2,3,6,7-tetrahydrospiro[furo[2,3-f]indole-3,4'-piperidine] (D8) and 2'-methyl-4'-(5-methyl-1,3,4-oxadiazol-2-yl)biphenyl-4-carboxylic acid (D9) using the procedure outlined in WO 96/19477 (23%). This was converted to the oxalate salt, which precipitated from acetone/ether as a white solid.

WORKUP

后处理

customprecipitated from acetone/ether as a white solid

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-f672babb6eb04180bd8898eb6dc3152c
来源数据集: uspto-grants-2000_08
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06107328
来源说明: uspto-grants-2000_08

反应 SMILES

[CH3:1][N:2]1[CH2:7][CH2:6][C:5]2([C:18]3[C:10](=[CH:11][C:12]4[CH2:13][CH2:14][NH:15][C:16]=4[CH:17]=3)[O:9][CH2:8]2)[CH2:4][CH2:3]1.[CH3:19][C:20]1[CH:25]=[C:24]([C:26]2[O:27][C:28]([CH3:31])=[N:29][N:30]=2)[CH:23]=[CH:22][C:21]=1[C:32]1[CH:37]=[CH:36][C:35]([C:38](O)=[O:39])=[CH:34][CH:33]=1>>[CH3:1][N:2]1[CH2:3][CH2:4][C:5]2([C:18]3[C:10](=[CH:11][C:12]4[CH2:13][CH2:14][N:15]([C:38]([C:35]5[CH:34]=[CH:33][C:32]([C:21]6[CH:22]=[CH:23][C:24]([C:26]7[O:27][C:28]([CH3:31])=[N:29][N:30]=7)=[CH:25][C:20]=6[CH3:19])=[CH:37][CH:36]=5)=[O:39])[C:16]=4[CH:17]=3)[O:9][CH2:8]2)[CH2:6][CH2:7]1