Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 913362Generated: October 31, 2026

Dimethylformamide → HCID 58965028, compound

https://huagongshe.com/reaction/913362

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantCesium carbonateHCID 10796—
Reactant3-(Iodomethyl)pyridine--hydrogen iodide (1/1)HCID 16213182—
ReactantHCID 67393211HCID 67393211—
SolventDichloromethaneHCID 6344—
ProductHCID 58965028HCID 5896502845.7%

Reaction Conditions

Temperature75 °C

Reaction Steps

A mixture of 4-amino-2-propylthiazolo[4,5-c]quinolin-7-ol acetate (318 mg, 1.0 mmol), cesium carbonate (1.3 g, 4.0 mmol), and DMF (20 mL) was stirred at 75° C. for 10 minutes. 3-(Iodomethyl)pyridine hydroiodide (381 mg, 1.1 mmol) was added in portions over a period of 3 hours. The heat source was removed and the reaction mixture was stirred at ambient temperature overnight. The reaction mixture was diluted with water (250 mL), stirred for 1 hour, and then filtered. The isolated solid was rinsed with water and then dried to provide a brown powder. This material was dissolved in dichloromethane and then purified by HPFC eluting with a gradient of 0-20% CMA in chloroform over 1400 mL and then 20% CMA in chloroform over 600 mL. The resulting solid was recrystallized from acetonitrile to provide 160 mg of 2-propyl-7-[(pyridin-3-yl)methoxy]thiazolo[4,5-c]quinolin-4-amine as an off-white solid, mp 167.0-169.0° C. MS (APCI) m/z 351 (M+H)+; Anal. calcd for C19H18N4OS: C, 65.12; H, 5.18; N, 15.99. Found C, 65.25; H, 5.06; N, 16.03.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08026366B2
Source datasetuspto-grants-2011_09
ORD IDord-5e26963a11c140c3affb89fa67ea67f4
Source noteuspto-grants-2011_09