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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636382Generated: October 31, 2026

1-Methylpiperazine → 3-Benzenesulphonyl-5-methyl-7-(4-methyl-piperazine-1-yl)-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/636382

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-MethylpiperazineHCID 53167—
Reactant3-Benzenesulphonyl-7-chloro-5-methyl-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidineHCID 10981097—
SolventDimethylformamideHCID 6228—
Product3-Benzenesulphonyl-5-methyl-7-(4-methyl-piperazine-1-yl)-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidineHCID 980208775.1%

Reaction Steps

0.15 g (1.5 mmol) of 1-methyl-piperazine in 10 ml of DMF was added to a solution of 0.45 g (1.275 mmol) of 3-benzenesulphonyl-7-chloro-5-methyl-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidine in 10 ml in DMF and stirred at 60° for 2 hrs. The reaction solution was cooled to RT and evaporated in a high vacuum. The residue was partitioned between 2N NaOH and CH2Cl2. The aqueous phase was extracted three times with CH2Cl2, and the combined organic phases were dried (MgSO4), filtered and evaporated. Subsequent chromatography (SiO2, CH2Cl2/MeOH 15:1) and crystallization from EtOH yielded 0.40 g (75%) of 3-benzenesulphonyl-5-methyl-7-(4-methyl-piperazine-1-yl) -2-methylsulphanyl-pyrazolo[1,5-a]pyrimidine as colorless crystals, m.p. 209-210°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194410B1
Source datasetuspto-grants-2001_02
ORD IDord-80c8f2b0cd684eb29595c2af0b498fc9
Source noteuspto-grants-2001_02