HRID467216

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CCc1c(COC(C)=O)[nH]c(C(=O)OCc2ccccc2)c1C

HCID3560140

未命名化合物

HCID10909563

3,4-DIETHYLPYRROLE

C8H13N

PRODUCTS

生成物

结构：CCc1c(Cc2[nH]c(Cc3[nH]c(C(=O)OCc4ccccc4)c(C)c3CC)c(CC)c2CC)[nH]c(C(=O)OCc2ccccc2)c1C

HCID13870527

未命名化合物

PROCEDURE

实验过程

condensing 3,4-diethylpyrrole with two molecular equivalents of benzyl-5-(acetoxymethyl)-4-ethyl-3-methylpyrrole-2-carboxylate to produce 2,5-bis(5-benzyloxycarbonyl-3-ethyl-4-methylpyrrol-2-ylmethyl)-3,4-diethylpyrrole;

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-f8a17c39a356443cab1cf43e7b06e20f
来源数据集: uspto-grants-1992_10
DOI: 10.6084/m9.figshare.5104873.v1
专利: US05159065
来源说明: uspto-grants-1992_10

反应 SMILES

[CH2:1]([C:3]1[C:7]([CH2:8][CH3:9])=[CH:6][NH:5][CH:4]=1)[CH3:2].[CH2:10]([O:17][C:18]([C:20]1[NH:21][C:22]([CH2:28]OC(=O)C)=[C:23]([CH2:26][CH3:27])[C:24]=1[CH3:25])=[O:19])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1>>[CH2:10]([O:17][C:18]([C:20]1[NH:21][C:22]([CH2:28][C:4]2[NH:5][C:6]([CH2:28][C:22]3[NH:21][C:20]([C:18]([O:17][CH2:10][C:11]4[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=4)=[O:19])=[C:24]([CH3:25])[C:23]=3[CH2:26][CH3:27])=[C:7]([CH2:8][CH3:9])[C:3]=2[CH2:1][CH3:2])=[C:23]([CH2:26][CH3:27])[C:24]=1[CH3:25])=[O:19])[C:11]1[CH:12]=[CH:13][CH:14]=[CH:15][CH:16]=1