Lithium hydroxide, monohydrate → {4-[1-(3-Chloro-benzenesulfonyl)-piperidin-4-yl]-6-fluoro-naphthalen-2-yl}-acetic acid

To a stirred solution of {4-[1-(3-chloro-benzenesulfonyl)-piperidin-4-yl]-6-fluoro-naphthalen-2-yl}-acetic acid methyl ester (90 mg, 0.19 mmol) in THF (4 mL) was added a solution of lithium hydroxide monohydrate (40 mg, 0.95 mmol) in water (1 mL) and the reaction mixture was stirred for 24 h at RT. The reaction mixture was concentrated under reduced pressure and washed with diethyl ether (3×5 mL). The washings were discarded. Water (5 mL) was added to the residue, and the mixture acidified (pH ˜2-3) with an aqueous solution of hydrochloric acid (2 N) and extracted with ethyl acetate (3×5 mL). The combined organic extracts were dried over Na2SO4 and evaporated under reduced pressure to give {4-[1-(3-chloro-benzenesulfonyl)-piperidin-4-yl]-6-fluoro-naphthalen-2-yl}-acetic acid (57 mg, 65%) as an off-white solid. 1H NMR (400 MHz, DMSO-d6) δ ppm 12.34 (br. s., 1H), 7.95 (dd, J=9.0, 6.1 Hz, 1H), 7.84-7.92 (m, 2H), 7.71-7.83 (m, 3H), 7.69 (s, 1H), 7.34-7.42 (m, 2H), 3.83 (d, J=11.2 Hz, 2H), 3.27-3.34 (m, 7H), 2.63 (t, J=11.2 Hz, 2H), 1.88-1.96 (m, 2H), 1.69-1.83 (m, 2H); MS cald. for C23H22ClFNO4S [(M−H)+]: 462, obsd. 462.2.

1. concentrationThe reaction mixture was concentrated under reduced pressure
2. washwashed with diethyl ether (3×5 mL)
3. additionWater (5 mL) was added to the residue
4. extractionextracted with ethyl acetate (3×5 mL)
5. dry with materialThe combined organic extracts were dried over Na2SO4
6. customevaporated under reduced pressure

ORD-Eintrag

ord-13f6644c30cb49309dea64638c4b3581

Quelldatensatz

uspto-grants-2014_04

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08691993B2