Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2402608Generated: October 29, 2026

N-Iodosuccinimide → 8-Chloro-3-cyclobutyl-1-iodoimidazo[1,5-a]pyrazine

https://huagongshe.com/reaction/2402608

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant8-Chloro-3-cyclobutylimidazo[1,5-a]pyrazineHCID 42609363—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product8-Chloro-3-cyclobutyl-1-iodoimidazo[1,5-a]pyrazineHCID 42609364—

Reaction Steps

8-Chloro-3-cyclobutylimidazo[1,5-a]pyrazine (1058 mg, 5.1 mmol) and NIS (1146 mg, 5.1 mmol) in anh DMF (10 mL) were stirred at 60° C. under Ar for 6 h. The reaction was diluted with DCM (˜400 mL), washed (H2O, brine), dried (Na2SO4) and concentrated under reduced pressure. Purification of the crude material by flash chromatography on silica gel (50 g cartridge, 10:1-8:1-7:1-6:1 hexanes:EtOAc) afforded the title compound as a pale yellow solid; 1H NMR (400 MHz, CDCl3) δ 7.51 (d, J=4.8 Hz, 1H), 7.26 (d, J=4.8 Hz, 1H), 3.75 (quintetd, J=1.2 Hz, 8.4 Hz, 1H), 2.62-2.42 (m, 4H), 2.32-1.98 (m, 2H); MS (ES+): m/z 334.0 (100) [MH+]; HPLC: tR=3.38 min (OpenLynx, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08796455B2
Source datasetuspto-grants-2014_08
ORD IDord-db6d469cd37f47dc9c8ef123c63e6bdd
Source noteuspto-grants-2014_08