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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1640554Generated: October 29, 2026

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

https://huagongshe.com/reaction/1640554

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 numberUS08114846B2
Source datasetuspto-grants-2012_02
ORD IDord-151625e24ebd4feda6ec691db470ce8b
Source noteuspto-grants-2012_02