Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333970Generated: October 25, 2026

Trifluoroacetic acid → 5-Methoxy-7-piperazin-1-yl-pyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/333970

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
Reactanttert-Butyl 4-(5-methoxy-pyrazolo[1,5-a]pyrimidin-7-yl)piperazine-1-carboxylateHCID 86691598—
SolventDichloromethaneHCID 6344—
Product5-Methoxy-7-piperazin-1-yl-pyrazolo[1,5-a]pyrimidineHCID 6683572975.3%

Reaction Steps

tert-Butyl 4-(5-methoxy-pyrazolo[1,5-a]pyrimidin-7-yl)piperazine-1-carboxylate (1.186 g, 3.56 mmol) was stirred for 10 minutes at room temperature in a 1:1 mixture of dichloromethane and trifluoroacetic acid. The mixture was evaporated to dryness under reduced pressure, the residue was dissolved in water, the resulting solution was washed with dichloromethane, basified with 4M NaOH and extracted with dichloromethane (3×). The combined organic phases were washed with water, dried over magnesium sulfate and the solvent was removed under reduced pressure to yield 624 mg of a solid (2.68 mmol, 75%). MS (APCI): m/z=234.1 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08883791B2
Source datasetuspto-grants-2014_11
ORD IDord-1388f3308109409084b28a3e1040c2d9
Source noteuspto-grants-2014_11