HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 62224Generated: October 30, 2026
HCID 136344401, compound → (5R,7S)-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/62224
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 136344401 | HCID 136344401 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (5R,7S)-2-bromo-5-(1,3-dimethyl-1H-pyrazol-4-yl)-7-(trifluoromethyl)-4,5,6,7-tetrahydropyrazolo[1,5-a]pyrimidine | HCID 136492823 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US09446046B2 |
|---|
| Source dataset | uspto-grants-2016_09 |
|---|
| ORD ID | ord-18011c0525094bd9bee9192a14ad720c |
|---|
| Source note | uspto-grants-2016_09 |
|---|