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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12595Generated: October 25, 2026

Sodium Methoxide → HCID 178447302, compound

https://huagongshe.com/reaction/12595

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium MethoxideHCID 10942334—
ReactantN-[(4-Bromophenyl)methyl]-N-(1-oxopentyl)-L-valineHCID 11696368—
ReactantHCID 178514830HCID 178514830—
CatalystTriphenylphosphineHCID 11776—
CatalystPalladium ChlorideHCID 24290—
SolventMethanolHCID 887—
ProductHCID 178447302HCID 17844730255.6%

Reaction Conditions

Temperature70 °C

Reaction Steps

Nitrogen is bubbled for 5 min. To a mixture made up of 0.50 g (1.35 mmol) of N-(4-bromobenzyl)-N-valeryl-L-valine, 0.308 g (1.52 mmol) of 2-(1H-tetrazol-5-yl)phenylboronic acid, 0.0028 g (0.016 mmol) of palladium chloride and 0.0084 g (0.032 mmol) of triphenylphosphine in a solution of 2.06 mL (13.0 mmol) of sodium methoxide in methanol al 30% and 5 mL of methanol are added. It is heated at 70° C. under nitrogen atmosphere for 5 h, 0.050 g of activated carbon is added and it is stirred at the same temperature for a further 15 min. After cooling to 20-25° C. it is filtered, the methanol is evaporated and it is treated with 25 mL of HCl 1N and 25 mL of AcOEt. The AcOEt phase is dried with anhydrous sodium sulphate and after distilling the solvent the crude product obtained is purified by silica gel chromatography (eluent AcOEt/heptane/AcOH 15:5:0.2) to provide 0.327 g (55.6%) of Valsartan.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07728021B2
Source datasetuspto-grants-2010_06
ORD IDord-193ceffdbb5248e78d55572665c91315
Source noteuspto-grants-2010_06