HRID1375611

反应详情

EQUATION

反应方程式

REACTANTS

反应物

结构：CN1CCN(c2cc(NC(=O)OC(C)(C)C)cc(C(F)(F)F)c2)CC1

HCID69244832

Carbamic acid, [3-(4-methyl-1-piperazinyl)-5-(trifluoromethyl)phenyl]-, 1,1-dimethylethyl ester

C17H24F3N3O2

结构：CC(C)(C)OC(=O)Nc1cc(N2CCOCC2)cc(C(F)(F)F)c1

HCID86606802

未命名化合物

PRODUCTS

生成物

HCID18543044

未命名化合物

PROCEDURE

实验过程

Utilising the procedure described in Example 90c, but employing [3-(4-methyl-1-piperazinyl)-5-(trifluoromethyl)phenyl]-carbamic acid, 1,1-dimethylethyl ester (Example 94a) in lieu of [3-(4-morpholinyl)-5-(trifluoromethyl)phenyl]-carbamic acid, 1,1-dimethylethyl ester, afforded the title compound as oil. 1H-NMR (400 MHz, DMSO-d6): 2.20 (s, 3H), 2.42 (m, 4H), 3.07 (m, 4H), 3.32 (br s, 2H), 5.34 (s, 1H) and 6.31 (s, 2H).