HRID1177101

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID588088

3,4-Difluorobenzaldehyde

C7H4F2O

结构：Cn1ccc(NC(=O)c2cc(O)c3c(c2)OC(C)(C)C3)n1

HCID59560084

未命名化合物

结构：COC(=O)c1cc(Oc2ccc(S(C)(=O)=O)cc2)cc2c1CC(C)O2

HCID59560437

未命名化合物

PRODUCTS

生成物

结构：Cn1ccc(NC(=O)c2cc(Oc3ccc(C=O)cc3F)c3c(c2)OC(C)(C)C3)n1

HCID59560083

未命名化合物

PROCEDURE

实验过程

The title compound was prepared in a similar manner as described for Intermediate 1f, from 3,4-difluoro-benzaldehyde and 4-hydroxy-2,2-dimethyl-2,3-dihydro-benzofuran-6-carbo-xylic acid (1-methyl-1H-pyrazol-3-yl)-amide (31a). 1H NMR (400 MHz, CDCl3) δ 9.92 (d, J=2.02 Hz, 1 H) 8.52 (s, 1 H) 7.72 (dd, J=10.36, 1.77 Hz, 1 H) 7.64 (d, J=8.34 Hz, 1 H) 7.28 (s, 1 H) 7.09 (t, J=7.96 Hz, 1 H) 7.05 (s, 1 H) 6.97 (s, 1 H) 6.77 (d, J=2.02 Hz, 1 H) 3.78 (s, 3 H) 2.98 (s, 2 H) 1.51 (s, 6 H); LCMS for C22H20FN3O4 m/z 410.00 (M+H)+.