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HRID237580

反应详情

EQUATION

反应方程式

HRID 237580 的结构方程式

REACTANTS

反应物

3
结构：COC(=O)C[C@@H]1COc2cc(O[C@@H]3CCc4c(Br)ccc(F)c43)ccc21
HCID86697103

未命名化合物

结构：COC(=O)C[C@@H]1COc2cc(O[C@@H]3CCc4c(B5OC(C)(C)C(C)(C)O5)ccc(F)c43)ccc21
HCID86697106

{(S)-6-[(R)-7-fluoro-4-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-indan-1-yloxy]-2,3-dihydro-benzofuran-3-yl}-acetic acid methyl ester

C26H30BFO6

结构：Cc1cc(-n2cncn2)cc(C)c1Br
HCID86697243

未命名化合物

PRODUCTS

生成物

1
结构：COC(=O)C[C@@H]1COc2cc(O[C@@H]3CCc4c(-c5c(C)cc(-n6cncn6)cc5C)ccc(F)c43)ccc21
HCID86697244

未命名化合物

PROCEDURE

实验过程

The title compound is prepared from methyl 2-((S)-6-((R)-7-fluoro-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-2,3-dihydro-1H-inden-1-yloxy)-2,3-dihydro-benzofuran-3-yl)acetate and 1-(4-bromo-3,5-dimethylphenyl)-1H-1,2,4-triazole following a procedure analogous to that described in Step 5 of Intermediate 1. LC (method 7): tR=1.16 min; Mass spectrum (ESI+): m/z=514 [M+H]+.