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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 887422Generated: October 30, 2026

Ammonium Chloride → (Rac)-trans-3-(3-fluoropyrazin-2-yl)cyclohexanol

https://huagongshe.com/reaction/887422

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium borohydrideHCID 4311764—
Reactant3-(3-Fluoropyrazin-2-yl)cyclohex-2-enoneHCID 59351405—
SolventMethanolHCID 887—
Product(Rac)-trans-3-(3-fluoropyrazin-2-yl)cyclohexanolHCID 59351407—
Product(Rac)-cis-3-(3-fluoropyrazin-2-yl)cyclohexanolHCID 66986535—

Reaction Steps

Sodium borohydride (295 mg, 7.80 mmol) was added was added portion wise to a solution of 3-(3-fluoropyrazin-2-yl)cyclohex-2-enone (500 mg, 2.60 mmol) in MeOH (15 ml) at RT. After completion of the addition the reaction mixture was stirred at RT for 30 minutes. It was then cooled in an ice-water bath, saturated aqueous ammonium chloride (25 ml) was added dropwise, and the resulting mixture was extracted with EtOAc (2×100 ml). The combined organic layers were washed with brine and dried over sodium sulfate. Filtration and concentration under reduced pressure, followed by flash chromatography on silica gel (0% to 20% EtOAc in hexanes) afforded (rac)-cis-3-(3-fluoropyrazin-2-yl)cyclohexanol and (rac)-trans-3-(3-fluoropyrazin-2-yl)cyclohexanol as colorless oils. MS (ESI, pos. ion) m/z: 197.0 (M+1) and MS (ESI, pos. ion) m/z: 197.0 (M+1), respectively. IC50 (uM) +++++.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08247418B2
Source datasetuspto-grants-2012_08
ORD IDord-73db3d5b9a4142b8b037c902370fec10
Source noteuspto-grants-2012_08