HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 12595Generated: October 25, 2026
Sodium Methoxide → HCID 178447302, compound
https://huagongshe.com/reaction/12595
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | N-[(4-Bromophenyl)methyl]-N-(1-oxopentyl)-L-valine | HCID 11696368 | — |
| Reactant | HCID 178514830 | HCID 178514830 | — |
| Catalyst | Triphenylphosphine | HCID 11776 | — |
| Catalyst | Palladium Chloride | HCID 24290 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 178447302 | HCID 178447302 | 55.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728021B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-193ceffdbb5248e78d55572665c91315 |
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| Source note | uspto-grants-2010_06 |
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