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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 244203Generated: October 30, 2026

N-Iodosuccinimide → 3-(8-Chloro-1-iodoimidazo[1,5-a]pyrazin-3-yl)-1-(hydroxymethyl)cyclobutanol

https://huagongshe.com/reaction/244203

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-IodosuccinimideHCID 120273—
Reactant3-(8-Chloroimidazo[1,5-a]pyrazin-3-yl)-1-(hydroxymethyl)cyclobutanolHCID 57681096—
SolventDimethylformamideHCID 6228—
Product3-(8-Chloro-1-iodoimidazo[1,5-a]pyrazin-3-yl)-1-(hydroxymethyl)cyclobutanolHCID 57681055—

Reaction Conditions

Temperature60 °C

Reaction Steps

Under inert atmosphere N-iodosuccinimide (3.6 g, 0.016 mol) and 3-(8-chloro-imidazo[1,5-a]pyrazin-3-yl)-1-hydroxymethyl-cyclobutanol (3.16 g, 0.012 mol) were dissolved in N,N-dimethylformamide (30 mL) and heated at 60° C. for 3.0 hours. The reaction mixture was then concentrated in vacuo to a dark oil and purified by HPFC Jones 20 g silica gel column, eluting with 5% MeOH:CH2Cl2 to yield a light brown fluffy solid which was triturated with diethyl ether and hexanes to afford the title compound; MS (ES+): m/z 379.85 (100) [MH+], 381.80 (30) [MH+]; HPLC: tR=2.30 min (OpenLynx, polar—5 min).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08653268B2
Source datasetuspto-grants-2014_02
ORD IDord-755bd782f6ec48c69372acb752c7ede0
Source noteuspto-grants-2014_02