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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 449008Generated: October 30, 2026

N-Iodosuccinimide → 8-Chloro-1-iodo-3-methylsulfanyl-imidazo[1,5-a]pyrazine

https://huagongshe.com/reaction/449008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant8-Chloro-3-(methylsulfanyl)imidazo[1,5-A]pyrazineHCID 59130382—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product8-Chloro-1-iodo-3-methylsulfanyl-imidazo[1,5-a]pyrazineHCID 5890198794%

Reaction Conditions

Temperature55 °C

Reaction Steps

P To a solution of 8-chloro-3-methylsulfanyl-imidazo[1,5-a]pyrazine (1.75 g, 0.00876 mol) in DMF (15 mL) was added N-iodosuccinimide (3.94 g, 0.0175 mol), the resulting mixture was stirred at 55° C. for 6 hrs. The mixture was diluted with EtOAc (200 mL), washed with sat. aq. NaHCO3 (40 mL), water (2×40 mL), brine (40 mL), and dried over anhydrous sodium sulfate. The crude material was purified by silica gel chromatography to give the title compound as a yellow solid, 2.68 g, 94% yield. 1H NMR (CDCl3, 400 MHz): δ 2.72 (s, 3H), 7.36 (d, J=4.8 Hz, 1H), 7.76 (d, J=4.8 Hz, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08481733B2
Source datasetuspto-grants-2013_07
ORD IDord-87439b1cffb448068234f536f9a05e83
Source noteuspto-grants-2013_07