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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 868999Generated: November 3, 2026

Ammonium Chloride → (3-Methylimidazo[2,1-f][1,6]naphthyridin-2-yl)methanol

https://huagongshe.com/reaction/868999

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium BicarbonateHCID 516892—
ReactantDiisobutylaluminumhydrideHCID 21225700—
ReactantMethyl 3-methylimidazo[2,1-f][1,6]naphthyridine-2-carboxylateHCID 70115494—
SolventDichloromethaneHCID 6344—
Product(3-Methylimidazo[2,1-f][1,6]naphthyridin-2-yl)methanolHCID 7011590450.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of methyl 3-methylimidazo[2,1-f][1,6]naphthyridine-2-carboxylate (100 mg, 0.39 mmol) in DCM (8 mL) was cooled to 0° C. Diisobutylaluminium hydride (1 M in cyclohexane, 1.2 mL, 1.2 mmol) was added dropwise over 10 min. Then the mixture was stirred at 0° C. for 1 h. 2 mL of saturated ammonium chloride aqueous solution was added slowly to quench the reaction. Then 5 mL of saturated sodium bicarbonate aqueous solution was added. The mixture was extracted with DCM (3×10 mL). The combined organic layers were dried over sodium sulfate, filtered, and concentrated to give the crude product. The crude product was purified by column chromatography to give 42 mg of the product as a yellow solid. MS (ESI) m/z 214.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08969349B2
Source datasetuspto-grants-2015_03
ORD IDord-308bca84d3d4470fa73d7a5ecc86d294
Source noteuspto-grants-2015_03