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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223237Generated: October 30, 2026

Methanol → HCID 178470992, compound

https://huagongshe.com/reaction/2223237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantBis(trimethylsilyl) phosphoniteHCID 10910816—
ReactantEthyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)acrylateHCID 54494317—
ReactantHCID 178418291HCID 178418291—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
ProductHCID 178470992HCID 17847099264%

Reaction Conditions

Temperature0 °C

Reaction Steps

Bis(trimethylsilyl)phosphonite was generated as described in WO 01/042252 using N,O-bis-(trimethylsilyl)acetamide (3.0 mL; 12.1 mmol) and ammonium hypophosphite (1.0 g; 12.0 mmol). The resulting reaction mixture was cooled to 0° C. and a solution of ethyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)acrylate (0.72 g; 2.35 mmol), in methylene chloride (4 mL) was added dropwise. The reaction was stirred overnight at room temperature. Methanol was added at 0° C. followed by water. The reaction mixture was concentrated. The remaining residue was dissolved in water and purified by preparative HPLC (0.1 M NH4Ac (aq)/CH3CN, 1/0→0/1), concentrated and lyophilized to afford 0.56 g (64%) of 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)-3-ethoxy-3-oxopropylphosphinic acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375121B2
Source datasetuspto-grants-2008_05
ORD IDord-7ec769bf8de94f5694e26620634af22e
Source noteuspto-grants-2008_05