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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348211Generated: October 31, 2026

Diisopropylethylamine → Diethyl 2-((3-(benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxamido)methyl)-5-fluorophenylphosphonate

https://huagongshe.com/reaction/348211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
ReactantDiethylphosphiteHCID 3780918—
ReactantN-(4-fluoro-2-iodobenzyl)-3-(benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxamideHCID 21070019—
CatalystTriphenylphosphineHCID 11776—
Catalystpalladium(II) acetateHCID 167845—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
ProductDiethyl 2-((3-(benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxamido)methyl)-5-fluorophenylphosphonateHCID 2106994251.3%

Reaction Conditions

Temperature80 °C

Reaction Steps

A solution of intermediate 174, N-(4-fluoro-2-iodobenzyl)-3-(benzyloxy)-9,9-dimethyl-4-oxo-4,6,7,9-tetrahydropyrimido[2,1-c][1,4]oxazine-2-carboxamide (0.200 g, 0.35 mmol) and triphenylphosphine (0.020 mg) in ethanol (5 ml) was flushed with argon and then treated with N,N-diisopropylethylamine (0.25 ml, 1.4 mmol), palladium(11) acetate (0.020 g) and diethyl phosphite (0.15 ml, 1.16 mmol). The reaction mixture was then sealed and heated at 80° C. for 18 h. The reaction mixture was then diluted with ethyl acetate, washed with 0.1 N hydrochloric acid, saturated sodium bicarbonate, brine, then dried over anhydrous magnesium sulfate and concentrated. Chromatography of the residue on silica gel (elution gradient of acetonitrile in dichloromethane) gave 0.103 g (51% yield) of the title compound as a white solid. 1HNMR 400 MHz (CDCl3) δ ppm: 1.36 (6H, t, J=6.6 Hz, 2×CH3), 1.64 (6H, s, 2×CH3), 4.04 (4H, m, 2×CH2), 4.08–4.22 (4H, m, 2×OCH2), 4.78 (2H, d, J=6.6 Hz, NCH2), 5.29 (2H, s, OCH2), 7.21 (1H, m, aromatic), 7.29–7.34 (3H, m, aromatics), 7.45–7.52 (3H, m, aromatics), 7.65–7.72 (1H, m, aromatic), 8.67 (1H, broad t, NH). HRMS (ESI+) calculated for C28 H34FN3O7P [M+H+]: 574.2118. Found: 574.2126.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176196B2
Source datasetuspto-grants-2007_02
ORD IDord-ad8b223c2b094379a2a5501a921bf68a
Source noteuspto-grants-2007_02