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HRID1675756

反应详情

EQUATION

反应方程式

HRID 1675756 的结构方程式

REACTANTS

反应物

2
结构：CC(C)(C)OC(=O)Cn1c(=O)[nH]c2ccccc21
HCID20814117

未命名化合物

结构：COC(=O)Cn1c(=O)n(CC(=O)OC(C)(C)C)c2cc(C)cc(C)c21
HCID86607784

未命名化合物

PRODUCTS

生成物

1
结构：COC(=O)Cn1c(=O)n(CC(=O)O)c2cc(C)cc(C)c21
HCID18449372

未命名化合物

PROCEDURE

实验过程

Essentially following the procedures described for Intermediate 7, but using tert-butyl [3-(2-methoxy-2-oxoethyl)-4,6-dimethyl-2-oxo-2,3-dihydro-1H-benzimidazol-1-yl]acetate from Step C in place of tert-butyl (2-oxo-3-pyridin-2-yl-2,3-dihydro-1H-benzimidazol-1-yl)acetate, the title compound was prepared. MS: m/z=293 (M+1).