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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1777916Generated: October 31, 2026

Water → 7-(Dimethoxymethyl)-1,2,3,4-tetrahydro-6-(methoxymethyl)-1,8-naphthyridine

https://huagongshe.com/reaction/1777916

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTetrahydrofuranHCID 8028—
ReactantSodium hydrideHCID 24758—
Reactant2-(Dimethoxymethyl)-5,6,7,8-tetrahydro-1,8-naphthyridine-3-methanolHCID 118036476—
Product7-(Dimethoxymethyl)-1,2,3,4-tetrahydro-6-(methoxymethyl)-1,8-naphthyridineHCID 118037123—

Reaction Steps

To a solution of (2-(dimethoxymethyl)-5,6,7,8-tetrahydro-1,8-naphthyridin-3-yl)methanol (intermediate 40, 94 mg, 0.394 mmol) in THF (2 ml) was added NaH (60% dispersion in mineral oil, 16.6 mg, 0.414 mmol). The resulting suspension was stirred at room temperature for 15 min, then Mel (0.026 ml, 0.414 mmol) was added and the reaction mixture was stirred for 28 h. The reaction mixture was poured into water and extracted with DCM (2×). The organic phase was then dried over Na2SO4, filtered and evaporated. The crude material was purified by normal phase chromatography (12 g silica gel cartridge, DCM/(DCM/MeOH 9/1) 100:0 to 50:50) to give the title compound as a yellow oil. (UPLC-MS 3) tR 0.51 min; ESI-MS 253.2 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09266883B2
Source datasetuspto-grants-2016_02
ORD IDord-7d15c25766be41949af1e0813e03ad66
Source noteuspto-grants-2016_02