Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636415Generated: October 30, 2026

Piperazine → HCID 21254934, compound

https://huagongshe.com/reaction/636415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantHCID 21255014HCID 21255014—
SolventDimethylformamideHCID 6228—
ProductHCID 21254934HCID 2125493427.7%

Reaction Steps

0.64 g (7.4 mmol) of piperazine in 10 ml of DMF was added to a solution of 1.0 g (3 mmol) of 3-benzenesulphonyl-7-chloro-2-ethyl-5-methyl-pyrazolo[1,5-a]pyrimidine in 10 ml of DMF and stirred at 60° for 2 hrs. The DMF was evaporated in a high vacuum, the residue was partitioned between 2N NaOH and CH2Cl2. The aqueous phase was extracted three times with 50 ml of CH2Cl2 and the combined organic phases were dried (MgSO4), filtered and evaporated. Subsequent chromatography (SiO2, CH2Cl2/MeOH 9:1) and crystallization from EtOH yielded 0.32 g (27%) of 3-benzenesulphonyl-2-ethyl-5-methyl-7-piperazin-1-yl-pyrazolo[1,5-a]pyrimidine as colorless crystals, m.p. 150-150.8°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194410B1
Source datasetuspto-grants-2001_02
ORD IDord-67facba39b0544efa7788c67a8d33dd3
Source noteuspto-grants-2001_02