تفاعل #2254175

ord-59dd127410f242638f8a69a43d6b1e44

معادلة التفاعل

CS(=O)(=O)Cl
methanesulfonyl chloride
CS(=O)(=O)N1C[C@@H](O)[C@H](O)[C@@H](C(F)F)C1
(3R,4R,5S)-5-(Difluoromethyl)-1-(methanesulfonyl)piperidine 3,4-diol
Cl.O[C@H]1[C@H](O)CNC[C@@H]1C(F)F
title compound
Cl.O[C@H]1[C@H](O)CNC[C@@H]1C(F)F
(3R,4R,5S)-5-(Difluoromethyl)piperidine 3,4-diol Hydrochloride

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىwas run at room temperature

الإجراء التجريبي

(3R,4R,5S)-5-(Difluoromethyl)-1-(methanesulfonyl)piperidine 3,4-diol (8b; Z=SO2; R5=Me). Following General Procedure D except that the reaction was run at room temperature and using methanesulfonyl chloride (0.16 g, 1.4 mmol), the title compound was obtained as a white solid (0.17 g, 51%). 1H NMR (DMSO-d6) 6.2 (t, 1H, J=53 Hz), 5.43 (d, 1H, ex), 5.38 (d, 1H, ex), 3.2-3.7 (m, 4H), 2.95 (s, 3H), 2.85 (m, 1H), 2.7 (t, 1H), 2.1 (br s, 1H). (3R,4R,5S)-5-(Difluoromethyl)-1-tosylpiperidine 3,4-diol (8b; Z=SO2; R5=Ph) Following General Procedure D except that the reaction was run at room temperature and using toluenesulfonyl chloride (0.26, 1.4 mmol), the title compound was obtained as a white solid (0.35 g, 67%). 1H NMR (DMSO-d6) 7.6 (d, 2H), 7.45 (d, 2H), 6.25 (t, 1H, J=53 Hz), 5.4 (2d, 2H, ex), 3.3-3.55 (m, 4H), 3.2 (m, 1H), 2.5 (m, 3H), 2.4 (t, 1H), 2.1 (m, 1H).

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US09044437B2uspto-grants-2015_06