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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1615697Generated: October 31, 2026

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

https://huagongshe.com/reaction/1615697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisobutylaluminum hydrideHCID 14487—
ReactantAmmonium ChlorideHCID 25517—
ReactantSodium BicarbonateHCID 516892—
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. DIBAL-H (1 M in cyclohexane, 1.2 mL, 1.2 mmol) was added dropwise over 10 min. 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, which was purified by column chromatography to give 42 mg of the product as a yellow solid. ESI MS: m/z 214.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765760B2
Source datasetuspto-grants-2014_07
ORD IDord-772da58aac7f43a3a3ca98201ba8afc8
Source noteuspto-grants-2014_07