Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705567Generated: October 30, 2026

Diethyl chlorophosphate → [5-Fluoro-2-(4-fluorobenzyloxy)pyrimidin-4-yl]phosphoramidic acid diethyl ester

https://huagongshe.com/reaction/705567

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl chlorophosphateHCID 13139—
ReactantSodium hydrideHCID 24758—
Reactant5-Fluoro-2-(4-fluorobenzyloxy)pyrimidin-4-amineHCID 57818574—
SolventTetrahydrofuranHCID 8028—
Product[5-Fluoro-2-(4-fluorobenzyloxy)pyrimidin-4-yl]phosphoramidic acid diethyl esterHCID 5781867311%

Reaction Steps

To a magnetically stirred solution of 5-fluoro-2-(4-fluorobenzyloxy)pyrimidin-4-ylamine (0.10 g, 0.42 mmol) in dry THF (5 mL) under a nitrogen atmosphere was added NaH (0.017 g of a 60 wt. % suspension, 0.42 mmol) and the mixture was stirred until bubbling ceased. Diethyl chlorophosphate (0.073 g, 0.42 mmol) was added dropwise, and the mixture was stirred at ambient temperature for 1 h. The reaction mixture was evaporated to dryness and the residue dissolved in EtOAc and washed saturated aqueous NH4Cl solution. The organic layer was separated, dried over Na2SO4, filtered, and evaporated. The crude material was purified on silica (acetone/CH2Cl2 gradient) to give 0.017 g (11%) of [5-fluoro-2-(4-fluorobenzyloxy)pyrimidin-4-yl]phosphoramidic acid diethyl ester as a white solid: mp 109-111° C.; 1H NMR (300 MHz, CDCl3) δ8.10 (t, J=1.8 Hz, 1H), 7.43 (m, 2H), 7.03 (t, J=8.5 Hz, 2H), 6.18 (br s, 1H), 5.35 (s, 2H), 4.25 (m, 4H), 1.38 (t, J=7.1 Hz, 6H); HPLC-MS (ESI) m/z 374 (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09174970B2
Source datasetuspto-grants-2015_11
ORD IDord-c95193a27b6e426aab1a9e76d69ec52e
Source noteuspto-grants-2015_11