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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192897Generated: October 30, 2026

Triethylamine → Methyl 2-(1-methyl-3-(4-pentylphenylsulfonamido)piperidin-3-yl)acetate

https://huagongshe.com/reaction/1192897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant4-t-Amylbenzenesulphonyl chlorideHCID 144625—
ReactantEthyl 2-(3-amino-1-methylpiperidin-3-yl)acetateHCID 58109960—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(1-methyl-3-(4-pentylphenylsulfonamido)piperidin-3-yl)acetateHCID 66865266—

Reaction Steps

A solution of ethyl 2-(3-amino-1-methylpiperidin-3-yl)acetate (52 mg, 0.28 mmol) and triethylamine (0.2 mL, 1.44 mmol) in dichlormethane (15 mL) was treated with 4-n-pentylbenzenesulfonly chloride (120 mg, 0.487 mmol). The resulting mixture was stirred overnight. After removal of the volatiles, the residue was redissolved in dichloromethane, washed with sat. NaHCO3, dried (Na2SO4), evaporated and purified by flash chromatography (eluent: EtOAc/hex 1:1 to EtOAc) to give the title compound. (95 mg, 86%) as colorless oil. 1H NMR (400 MHz, CDCl3) δ 7.80 (d, 2H, J=8.0 Hz), 7.27 (d, 2H, J=8.0 Hz), 5.67 (brs, 1H), 3.55 (s, 3H), 2.84 (d, 1H, J=11.6 Hz), 2.73-2.60 (m, 4H), 2.47 (brs, 1H), 2.20-1.92 (m, 6H; NCH3 and 3H), 1.70-1.57 (m, 3H), 1.48-1.27 (m, 6H), 0.88 (t, 3H, J=7.2 Hz); MS 397.2 ESI [M+H]+, calcd for [C20H32N2O4S+H]+ 397.22

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680282B2
Source datasetuspto-grants-2014_03
ORD IDord-881d44fc4c1745218aaa83cb9ee2e349
Source noteuspto-grants-2014_03