HRID332970

反应详情

EQUATION

反应方程式

REACTANTS

反应物

HCID2734688

Benzenacetyl chloride, 4-methoxy-

C9H9ClO2

结构：Cl.NC1=NS(=O)(=O)Nc2cccc(OC[C@H]3CCCC[NH2+]3)c21

HCID86714283

未命名化合物

PRODUCTS

生成物

结构：COc1ccc(CC(=O)N2CCCC[C@@H]2COc2cccc3c2C(N)=NS(=O)(=O)N3)cc1

HCID86714292

未命名化合物

收率 14%

PROCEDURE

实验过程

Prepared as in Example 8 from (R)-2-(((4-amino-2,2-dioxido-1H-benzo[c][1,2,6]thiadiazin-5-yl)oxy)methyl)piperidinium hydrochloride (Example 15a) and 2-(4-methoxyphenyl)acetyl chloride in 14% yield. 1H NMR (DMSO-d6, 400 MHz, 80° C.): 1.15-1.29 (m, 1H), 1.44-1.65 (m, 4H), 1.70-1.78 (m, 1H), 3.01 (m, 1H), 3.66 (s, 2H), 3.70 (s, 3H), 3.90 (br s, 1H), 4.19 (br s, 1H), 4.43 (t, J=12 Hz, 1H), 5.03 (br s, 1H), 5.64 (d, J=8 Hz, 1H), 6.80 (t, J=8 Hz, 3H), 7.13 (d, J=8 Hz, 2H), 7.41 (t, J=8 Hz, 1H), 7.81 (br s, 2H), 10.63 (s, 1H). M+H=459.