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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 748513Generated: October 28, 2026

1-Benzylpiperazine → HCID 26945817, compound

https://huagongshe.com/reaction/748513

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-BenzylpiperazineHCID 75994—
Reactant2-Chloro-5-pyridinesulfonyl chlorideHCID 2792792—
SolventDichloromethaneHCID 6344—
ProductHCID 26945817HCID 2694581782%

Reaction Steps

To a solution of benzylpiperazine (0.45 mL, 2.59 mmol) in methylene chloride (15 mL), cooled on an ice-bath, was 6-chloropyridine-3-sulfonyl chloride (0.50 g, 2.36 mmol; described in: Naegeli, C. et al. Helv. Chim. Actal. 1938, 21, 1746-1750) dissolved in methylene chloride (10 mL) added slowly. The reaction was stirred for 30 min and the formed white precipitation was filtered and washed with methylene chloride and water affording, after drying, 0.68 g (82% yield) of the title compound: 1H NMR (DMSO-d6, 400 MHz) δ 8.70 (d, J=3 Hz, 1 H), 8.14 (dd, J=8, 3 Hz, 1 H), 7.76 (d, J=8 Hz, 1 H), 7.50-7.43 (m, 2 H), 7.38-7.30 (m, 3 H), 4.23 (br s, 2 H), 3.79-3.63 (m, 2 H), 3.45-3.18 (m, 2 H), 3.11-2.96 (m, 2 H), 2.96-2.81 (m, 2 H); MS (ES) m/z 352 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07399780B2
Source datasetuspto-grants-2008_07
ORD IDord-dc4c0e7bab0b40f7911ebf85d1fcc03f
Source noteuspto-grants-2008_07