HRID50353

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID313

Hydrochloric Acid

ClH

HCID517111

Ammonium carbonate

CH8N2O3

结构：COC(=O)CCN(C(=O)c1cnc2c(c1)nc(CSc1ccc(C#N)cc1)n2C)c1ccccc1

HCID18412655

未命名化合物

HCID86587043

未命名化合物

PRODUCTS

生成物

结构：CCOC(=O)CCN(C(=O)c1cnc2c(c1)nc(CSc1ccc(C(=N)N)cc1)n2C)c1ccccc1.Cl

HCID18412390

未命名化合物

收率 88%

AUXILIARIES

试剂、催化剂与溶剂

溶剂HCID702

Ethanol

C2H6O

PROCEDURE

实验过程

Prepared analogously to Example 1 from 3-methyl-2-[(4-cyanophenyl)thiomethyl]imidazo[4,5-b]pyridin-6-yl-carboxylic acid-N-phenyl-N-(2-methoxycarbonylethyl)amide, ethanolic hydrochloric acid, ethanol, and ammonium carbonate. Yield: 88% of theory, C27H28N6O3S (516.63); Rf value: 0.23 (silica gel; ethyl acetate/ethanol/ammonia=50:45:5); EKA mass spectrum: (M+H)+=517; (M+H+Na)++=270.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-5ea9f7c83c2347fba7b0305cd5780c26
来源数据集: uspto-grants-2004_03
DOI: 10.6084/m9.figshare.5104873.v1
专利: US06710055B2
来源说明: uspto-grants-2004_03

反应 SMILES

[C:1]1([N:7]([CH2:30]CC(OC)=O)[C:8]([C:10]2[CH:11]=[C:12]3[N:18]=[C:17]([CH2:19][S:20][C:21]4[CH:26]=[CH:25][C:24]([C:27]#[N:28])=[CH:23][CH:22]=4)[N:16]([CH3:29])[C:13]3=[N:14][CH:15]=2)=[O:9])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[ClH:36].C(=O)([O-])[O-].[NH4+:41].[NH4+].[C:43]([O:46][CH2:47][CH3:48])(=[O:45])[CH3:44].C(O)C.N>C(O)C>[ClH:36].[C:1]1([N:7]([CH2:30][CH2:44][C:43]([O:46][CH2:47][CH3:48])=[O:45])[C:8]([C:10]2[CH:11]=[C:12]3[N:18]=[C:17]([CH2:19][S:20][C:21]4[CH:22]=[CH:23][C:24]([C:27](=[NH:28])[NH2:41])=[CH:25][CH:26]=4)[N:16]([CH3:29])[C:13]3=[N:14][CH:15]=2)=[O:9])[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=1