HRID67142

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID12806652

未命名化合物

PRODUCTS

生成物

HCID178465854

未命名化合物

PROCEDURE

实验过程

6-methyl-5-propionyl-benzimidazole-2-carboxylic acid; 6-methyl-5-valeryl-benzimidazole-2-carboxylic acid; 5(6)-butyryl-benzimidazole-2-carboxylic acid; 5-butyryl-6-methoxy-benzimidazole-2-carboxylic acid; 5-butyryl-6-chloro-benzimidazole-2-carboxylic acid; 5-cyclopropylcarbonyl-6-methyl-benzimidazole-2-carboxylic acid; 5-cyclohexylcarbonyl-6-methyl-benzimidazole-2-carboxylic acid; 5-(4-methoxy-butyryl)-6-methyl-benzimidazole-2-carboxylic acid; 6-methyl-5-(4-methylthio-butyryl)-benzimidazole-2-carboxylic acid; 6-methyl-5-(4-methylsulphinyl-butyryl)-benzimidazole-2-carboxylic acid; 6-methyl-5-(4-phenylthio-butyryl)-benzimidazole-2-carboxylic acid; 6-methyl-5-(4-phenylsulphinyl-butyryl)-benzimidazole-2-carboxylic acid; and methyl 5-butyryl-6-methyl-benzimidazole-2-carboxylate.

来源与证据

来源类型: Open Reaction Database
ORD 记录: ord-ade6f74779e04463a800fe24164fff4e
来源数据集: uspto-grants-1982_08
DOI: 10.6084/m9.figshare.5104873.v1
专利: US04344957
来源说明: uspto-grants-1982_08

反应 SMILES

[CH3:1][C:2]1[C:3]([C:14](=[O:17])[CH2:15]C)=[CH:4][C:5]2[NH:9][C:8]([C:10]([OH:12])=[O:11])=[N:7][C:6]=2[CH:13]=1.CC1C(C(=O)CCCC)=CC2NC(C(O)=O)=NC=2C=1.C(C1C(OC)=CC2N=C(C(O)=O)NC=2C=1)(=O)CCC.C(C1C(Cl)=CC2N=C(C(O)=O)NC=2C=1)(=O)CCC.C1(C(C2C(C)=CC3N=C(C(O)=O)NC=3C=2)=O)CC1.C1(C(C2C(C)=CC3N=C(C(O)=O)NC=3C=2)=O)CCCCC1.COCCCC(C1C(C)=CC2N=C(C(O)=O)NC=2C=1)=O.CC1C(C(=S)CCCC)=CC2NC(C(O)=O)=NC=2C=1.CC1C(C(=O)CCCS(C)=O)=CC2NC(C(O)=O)=NC=2C=1.CC1C(C(=S)CCCC2C=CC=CC=2)=CC2NC(C(O)=O)=NC=2C=1.CC1C(C(=O)CCCS(C2C=CC=CC=2)=O)=CC2NC(C(O)=O)=NC=2C=1.C(C1C(C)=CC2N=C(C(OC)=O)NC=2C=1)(=O)CCC>>[C:14]([C:3]1[C:2]([CH3:1])=[CH:13][C:6]2[N:7]=[C:8]([C:10]([OH:12])=[O:11])[NH:9][C:5]=2[CH:4]=1)(=[O:17])[CH3:15]