Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 493874Generated: October 31, 2026

Ammonia → 3-Cyclobutyl-1-iodoimidazo[1,5-a]pyrazin-8-amine

https://huagongshe.com/reaction/493874

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant8-Chloro-3-cyclobutyl-1-iodoimidazo[1,5-a]pyrazineHCID 42609364—
SolventIsopropanolHCID 3776—
Product3-Cyclobutyl-1-iodoimidazo[1,5-a]pyrazin-8-amineHCID 42609365—

Reaction Conditions

Temperature115 °C

Reaction Steps

A Parr bomb containing 8-chloro-3-cyclobutyl-1-iodoimidazo[1,5-a]pyrazine (759 mg, 2.3 mmol) in IPA (100 mL) was saturated with NH3(g) for 5 min at 0° C. then sealed and heated at 115° C. for 38 h. The reaction mixture was then concentrated under reduced pressure, partitioned between DCM (200 mL) and H2O (50 mL) and extracted with DCM (50 mL). Combined organic fractions were washed with brine, dried (Na2SO4) and concentrated under reduced pressure to provide the title compound as a white solid; 1H NMR (400 MHz, CDCl3) δ 7.13 (d, J=4.8 Hz, 1H), 7.01 (d, J=5.2 Hz, 1H), 5.63 (br, 2H), 3.73 (quintetd, J=0.8 Hz, 8.4 Hz, 1H), 2.60-2.38 (m, 4H), 2.20-1.90 (m, 2H); MS (ES+): m/z 315.9 (100) [MH+]; HPLC: tR=1.75 min (OpenLynx, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07534797B2
Source datasetuspto-grants-2009_05
ORD IDord-51720be4b5704858965a9fb80b8fec78
Source noteuspto-grants-2009_05