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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1043015Generated: October 25, 2026

Methoxyacetyl chloride → HCID 52934277, compound

https://huagongshe.com/reaction/1043015

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethoxyacetyl chlorideHCID 96623—
ReactantSodium BicarbonateHCID 516892—
Reactant7-(3,5-dimethyl-4-isoxazolyl)-6-(methoxy)-N4-(2-pyridinylmethyl)-3,4-quinolinediamineHCID 67207131—
SolventDichloromethaneHCID 6344—
ProductHCID 52934277HCID 52934277—

Reaction Conditions

Temperature0 °C

Reaction Steps

7-(3,5-dimethylisoxazol-4-yl)-6-methoxy-N4-(pyridin-2-ylmethyl)quinoline-3,4-diamine (for a preparation see Intermediate 63, 500 mg) was dissolved in DCM (20 ml) and the reaction mixture was cooled to 0° C. 2-Methoxyacetyl chloride (1.1 eq) was added dropwise and the reaction mixture was stirred at room temperature for 30 min. The mixture was hydrolysed using a solution of sodium hydrogen carbonate and extracted with DCM. The organic was dried over Na2SO4, filtered and concentrated to dryness. The obtained residue was dissolved in acetic acid (5 ml) and the reaction mixture was heated to 130° C. for 16 h. The reaction mixture was treated with sodium hydroxide (1M) and extracted with DCM. The organic was dried over Na2SO4, filtered and concentrated to dryness. The residue was purified by chromatography on silica gel, eluting with DCM/methanol (95:5). The resulting compound was recrystallised from acetonitrile and dried under vacuum to give 4-(8-methoxy-2-(methoxymethyl)-1-(pyridin-2-ylmethyl)-1H-imidazo[4,5-c]quinolin-7-yl)-3,5-dimethylisoxazole (50 mg) as a cream-coloured powder.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08557984B2
Source datasetuspto-grants-2013_10
ORD IDord-f93046ae0dbf4c04929e1f8dbad45c49
Source noteuspto-grants-2013_10