Reaktion #1723676

Reaktionsgleichung

2-chlorobenzenesulfonic acid 1-[[1-N-(tert-butoxycarbonyl)piperidin-4-yl]methoxy]naphthalen-3-yl ester

HCl

→

title compound

2-Chlorobenzenesulfonic acid 1-[(piperidin-4-yl)methoxy]naphthalen-3-yl ester hydrochloride

Lösungsmittel

methylene chloride

dioxane

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigetriturated with diethyl ether

Vorschrift

To a solution of 319 mg (0.596 mmol) of 2-chlorobenzenesulfonic acid 1-[[1-N-(tert-butoxycarbonyl)piperidin-4-yl]methoxy]naphthalen-3-yl ester, as prepared in the preceding step, in 2 mL of methylene chloride was added 1.5 mL (6 mmol) of 4N HCl in dioxane. The reaction mixture was stirred for 1 h and triturated with diethyl ether to afford 281 mg of the title compound as a colorless powder. 1H-NMR (300 MHz, DMSO-d6) δ 8.94 (bd, 1H, J=9 Hz), 8.68 (bd, 1 H, J=10 Hz), 8.6 (d, 1H, J=8 Hz), 7.8-7.98 (m, 4 Hz), 7.50-7.6 (m, 3H), 7.18 (d, 1H, J=2 Hz), 6.69 (d, 1H, J=2H), 3.94 (d, 2H, J=7 Hz), 2.93 (q,2 H), 2.16 (bm, 1H), 1.96 (d, 2H), and 1.57-1.71 (m, 2H). Mass spectrum (MALDI-TOF; gentisic acid matrix) calcd. for C22H22ClNO4S: 432.1 (M+H). Found: 431.5.

Quelle