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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 643384Generated: October 30, 2026

3-(1-Bromo-8-chloroimidazo[1,5-a]pyrazin-3-yl)cyclobutanone → 3-(1-Bromo-8-chloroimidazo[1,5-A]pyrazin-3-YL)-1-methylcyclobutanol

https://huagongshe.com/reaction/643384

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-(1-Bromo-8-chloroimidazo[1,5-a]pyrazin-3-yl)cyclobutanoneHCID 16119327—
ReactantHCID 178418332HCID 178418332—
SolventTetrahydrofuranHCID 8028—
Product3-(1-Bromo-8-chloroimidazo[1,5-A]pyrazin-3-YL)-1-methylcyclobutanolHCID 53328622—

Reaction Conditions

Temperature-78 °C

Reaction Steps

3-(1-Bromo-8-chloroimidazo[1,5-a]pyrazin-3-yl)cyclobutanone (51.988 g, 0.17 mol) in anhydrous THF (550 g, 620 mL) under nitrogen at −78° C. was treated with a 3.0 M solution of methyl magnesium chloride in THF (130 mL, 0.38 mol) over 30 min. The mixture was stirred at −78° C. for 30 min and then the cooling bath was removed and the mixture quenched with 14% NH4Cl (132 g). EtOAc was added to the aqueous phase and the pH was adjusted to −5 with 20% HCl and the layers separated. The combined organic phases were concentrated in vacuo to a slurry and 0.5 L of toluene was added and the mixture concentrated in vacuo until the EtOAc was removed. The slurry was heated at reflux until homogeneous then allowed to cool to provide desired product, which was isolated by filtration and dried in vacuo. 1H NMR (DMSO-d6, 400 MHz): δ 1.37 (s, 3H), 2.35-2.49 (m, 4H), 3.52 (dddd, 1H, J=9.6, 9.6, 9.6, 9.6 Hz), 5.18 (bs, 1H), 7.37 (d, 1H, J=5.2 Hz) and 8.26 (d, 1H, J=5.2 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07700594B2
Source datasetuspto-grants-2010_04
ORD IDord-2c21f1475ad249d0a9ef96b954d1b3ad
Source noteuspto-grants-2010_04