Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62223Generated: October 30, 2026

HCID 136344401, compound → (5S,7R)-2-bromo-5-(1,3-dimethyl-1H-pyrazol-4-yl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine

https://huagongshe.com/reaction/62223

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 136344401HCID 136344401—
SolventMethanolHCID 887—
Product(5S,7R)-2-bromo-5-(1,3-dimethyl-1H-pyrazol-4-yl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidineHCID 136492809—

Reaction Steps

The racemic 2-bromo-5-(1,3-dimethyl-1H-pyrazol-4-yl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine (1.5 g, 4.1 mmol, Preparation 8) was dissolved in methanol (35 mL) and the cloudy solution was gently warmed providing a clear solution. The solution was then filtered through a medium porosity Buchner funnel. The clear filtrate was directly used for chiral HPLC purification. 1 mL of this solution was loaded onto a 2.1 cm×25 cm Chiralcel OD column and eluted with a mobile phase comprising of isopropyl alcohol and methanol (1:1 ratio) at a flow rate of 15 mL/min. The two (R and S) enantiomers were collected separately. 27 such injections were carried out and the pooled fractions of pure (R and S) enantiomers were concentrated under reduced pressure. The title compound was isolated as a white powder (0.71 g, 1.95 mmols, >95% ee).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09446046B2
Source datasetuspto-grants-2016_09
ORD IDord-89f010a9190546d899398e67cb5addbb
Source noteuspto-grants-2016_09