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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1444722Generated: October 30, 2026

Piperidine → 2-[3-oxo-1-(toluene-4-sulfonyl)-1,2,3,4-tetrahydro-pyrazin-2-yl]-N-[2-(4-piperidin-1-ylmethyl-phenyl)-ethyl]-acetamide

https://huagongshe.com/reaction/1444722

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperidineHCID 8082—
ReactantN-[2-(4-chloromethyl-phenyl)-ethyl]-2-[3-oxo-1-(toluene-4-sulfonyl)-1,2,3,4-tetrahydro-pyrazin-2-yl]-acetamideHCID 68682701—
SolventDichloromethaneHCID 6344—
Product2-[3-oxo-1-(toluene-4-sulfonyl)-1,2,3,4-tetrahydro-pyrazin-2-yl]-N-[2-(4-piperidin-1-ylmethyl-phenyl)-ethyl]-acetamideHCID 68678236—

Reaction Steps

To a solution of N-[2-(4-chloromethyl-phenyl)-ethyl]-2-[3-oxo-1-(toluene-4-sulfonyl)-1,2,3,4-tetrahydro-pyrazin-2-yl]-acetamide (195 mg, 0.42 mmol) in CH2Cl2 (2 mL) was added piperidine (Aldrich, 0.13 mL, 1.3 mmol) at rt. The reaction mixture was stirred at rt overnight and then diluted with CH2Cl2 (50 mL). The organic solution was washed with saturated NaHCO3, and brine, dried over Na2SO4, filtered and concentrated in vacuo. Purification by preparative TLC (7% MeOH—CH2Cl2) afforded the title compound. MS (ESI): 511 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07662811B2
Source datasetuspto-grants-2010_02
ORD IDord-6fd74f8e79b547488ba515ab440634a5
Source noteuspto-grants-2010_02