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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1192916Generated: November 1, 2026

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

https://huagongshe.com/reaction/1192916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2-Chloroethyl chlorosulfonylcarbamateHCID 13118812—
ReactantN-methyl-4-octylanilineHCID 17827013—
ReactantMethyl 2-(3-amino-1-methylpiperidin-3-yl)acetateHCID 66864584—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
ProductMethyl 2-(1-methyl-3-(N-methyl-N-(4-octylphenyl)sulfamoylamino)piperidin-3-yl)acetateHCID 6686493922%

Reaction Steps

To a solution of methyl 2-(3-amino-1-methylpiperidin-3-yl)acetate (186 mg, 1 mmol) and Et3N (0.42 mL, 3 mmol) in CH2Cl2 was added the solution of 2-chloroethyl chlorosulfonylcarbamate in CH2Cl2 (0.77 M, 1.3 mL, 1 mmol). After addition, the resulting mixture was stirred overnight at rt. Evaporation of solvents gave a light yellow oil which was used without further purification. A solution of this crude mixture, N-methyl-4-octylaniline (241 mg, 1.1 mmol) and Et3N (0.42 mL, 3 mmol) in CH3CN (10 mL) was refluxed for 2 h. After cooling to rt and evaporating solvents, the residue was purified by a short column (EtOAc/hexance=10:1) to give the title compound (105 mg, 22%) as white solid. MS ESI 468.3 [M+H]+, calcd for [C24H41N3O4S+H]+ 468.29.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08680282B2
Source datasetuspto-grants-2014_03
ORD IDord-db0448d255ff46a59408ab78dcf93b73
Source noteuspto-grants-2014_03