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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1789728Generated: October 27, 2026

Sodium Hydroxide → 3,4-Dihydro-2H-pyrido[3,2-b]-1,4-oxazin-2-ylmethanol

https://huagongshe.com/reaction/1789728

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantEthyl 3-oxo-3,4-dihydro-2H-pyrido[3,2-B][1,4]oxazine-2-carboxylateHCID 12079662—
ReactantAluminium lithium hydrideHCID 21226445—
SolventTetrahydrofuranHCID 8028—
Product3,4-Dihydro-2H-pyrido[3,2-b]-1,4-oxazin-2-ylmethanolHCID 22036434—

Reaction Conditions

Temperature45 °C

Reaction Steps

A solution of 3,4-dihydro-3-oxo-2H-pyrido[3,2-b]-1,4-oxazin-2-carboxylic acid ethyl ester (1.10 g, 5.0 mmol) in THF (50 mL) was added over 5 min to a stirred mixture of LiAlH4 (0.38 g, 10 mmol) and THF (20 mL) at 40° C. The mixture was stirred at 45° C. for 30 min and at reflux for 4 h. The mixture was allowed to attain room temperature and excess LiAlH4 decomposed with 50% aqueous NaOH. The mixture was filtered through Celite, and the filtrate was concentrated. The residue (0.42 g) was extracted with CH2Cl2 and the extract was concentrated and purified by chromatography on silica gel (gradient: PhMe to PhMe/MeOH/Et3N, 8:1:1) to give the product as a white solid: yield 0.11 g (13%); mp 123-124° C. Anal. (C8H10N2O2) C, H, N.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07071180B2
Source datasetuspto-grants-2006_07
ORD IDord-505c56af85be4a3496e51b1ff750ab27
Source noteuspto-grants-2006_07