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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 636452Generated: October 31, 2026

Phosphorus oxychloride → 3-Benzenesulphonyl-7-chloro-5-(4-methyl-piperazin-1-ylmethyl)-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/636452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantHCID 178503604HCID 178503604—
Product3-Benzenesulphonyl-7-chloro-5-(4-methyl-piperazin-1-ylmethyl)-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidineHCID 2125505198%

Reaction Steps

A suspension of 4.0 g (9 mmol) of 3-benzenesulphonyl-5-(4-methyl-piperazin-1-ylmethyl)-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidin-7-ol in 100 ml of POCl3 was heated at reflux for 3 hrs. The reaction solution was cooled to RT and evaporated. The residue was treated with 100 ml of ice-water and the pH value of the solution was adjusted to 8 with sat. NaHCO3 solution. The aqueous phase was extracted three times with 150 ml of CH2Cl2 and the organic phases were dried (MgSO4), filtered and evaporated. Chroma-tography (SiO2CH2Cl2/MeOH 10:1) of the residue yielded 4.0 g (98%) of 3-benzenesulphonyl-7-chloro-5-(4-methyl-piperazin-1-ylmethyl)-2-methylsulphanyl-pyrazolo[1,5-a]pyrimidine as a pale brown powder, m.p. 113-116°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06194410B1
Source datasetuspto-grants-2001_02
ORD IDord-5777293b18964bf8bf6d27f9c2d1e97d
Source noteuspto-grants-2001_02