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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192900Generated: October 31, 2026

Triethylamine → Methyl 2-(1-methyl-3-(N-(4-octylphenyl)sulfamoylamino)piperidin-3-yl)acetate

https://huagongshe.com/reaction/1192900

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-chloroethyl N-(4-octylphenyl)sulfamoylcarbamateHCID 58109976—
Reactant2-(3-Amino-1-methylpiperidin-3-yl)acetateHCID 86649846—
SolventAcetonitrileHCID 6342—
ProductMethyl 2-(1-methyl-3-(N-(4-octylphenyl)sulfamoylamino)piperidin-3-yl)acetateHCID 6686449427.4%

Reaction Steps

A solution of 2-chloroethyl N-(4-octylphenyl)sulfamoylcarbamate (156 mg, 0.4 mmol) in CH3CN (10 mL) was treated with Et3N (0.14 mL, 1 mmol) and refluxed for 25 min. and cooled. A solution of 2-(3-amino-1-methylpiperidin-3-yl)acetate (62 mg, 0.33 mmol) was added and the resulting mixture was refluxed for 4 h. After removal of the solvent in vacuo, the residue was dissolved in dichloromethane (40 mL) and washed with sat. NaHCO3 (10 mL), H2O (10 mL), brine (10 mL) and dried (Na2SO4). After evaporation, the residue was purified by flash chromatography (EtOAc/hex 1:4 to EtOAc) to give the title compound (41 mg, 27%) as colorless oil. MS ESI 454.3[M+H]+, calcd for [C23H39N3O4S+H]+ 454.27.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680282B2
Source datasetuspto-grants-2014_03
ORD IDord-fd1b85da27084615b130ce0d77af19db
Source noteuspto-grants-2014_03