Hydrochloric Acid → 2-Chlorobenzenesulfonic acid 3-[(piperidin-4-yl)methoxy]-5-methylphenyl ester

HRID 1636481Notes

Reaction equation

HRID 1636481 reaction equation
C(OC([N:8]1[CH2:13][CH2:12][CH:11]([CH2:14][O:15][C:16]2[CH:17]=[C:18]([O:23][S:24]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=3[Cl:33])(=[O:26])=[O:25])[CH:19]=[C:20]([CH3:22])[CH:21]=2)[CH2:10][CH2:9]1)=O)(C)(C)C.Cl>O1CCOCC1>[NH:8]1[CH2:13][CH2:12][CH:11]([CH2:14][O:15][C:16]2[CH:17]=[C:18]([O:23][S:24]([C:27]3[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=3[Cl:33])(=[O:25])=[O:26])[CH:19]=[C:20]([CH3:22])[CH:21]=2)[CH2:10][CH2:9]1

Participants

4

Procedure

2-Chlorobenzenesulfonic acid 3-[[N-(tert-butoxycarbonyl)piperidin-4-yl]methoxy]-5-methylphenyl ester (745 mg, 1.5 mmol), as prepared in the preceding step, was treated with 4N HCl in 1,4-dioxane (20 mL) at room temperature for 2 h. The solvent was removed in vacuo and the residue was purified by flash column chromatography (10% methanol in methylene chloride saturated with NH3) to give the title compound as a colorless syrup (570 mg, 95%). 1H-NMR (300 MHz, CDCl3) δ 1.45 (m, 1H), 1.94 (m, 3H), 2.23 (s,3H), 2.45 (m, 1H), 2.71 (dt, 2H, J=1.2, 12.3 Hz), 3.51 (m, 2H), 3.76 (m, 2H), 6.46 (t, 1H, J=2.1 Hz), 6.53 (s, 1H), 6.58 (s, 1H), 7.40 (t, 1H, J=6.5 Hz), 7.62 (m, 2H), and 7.97 (dd, 1H, J=1.4, 7.9 Hz). Mass spectrum (MALDI-TOF, sinapinic acid matrix) calcd. for C19H22NO4SCl: 396.1 (M+H), Found: 396.4.

Workup

  1. customThe solvent was removed in vacuo
  2. customthe residue was purified by flash column chromatography (10% methanol in methylene chloride saturated with NH3)

Sources & evidence

ORD record
ord-9d1db8e41fa94253b219d18937919e71
Source dataset
uspto-grants-2000_03
Patent number
US06034127

Reaction notes

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