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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 584946Generated: October 30, 2026

Hydrochloric Acid → HCID 22341474, compound

https://huagongshe.com/reaction/584946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantMethanolHCID 887—
ReactantSodium HydroxideHCID 14798—
ReactantHCID 10224625HCID 10224625—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22341474HCID 2234147446%

Reaction Steps

180 mg (0.4 mmol) of methyl 2-(3′-{[methyl-(1-phenylmethanoyl)amino]methyl}biphenyl-4-ylmethyl)malonamate (prepared in Example 16(d)) in 2 ml of methanol, 2 ml of tetrahydrofuran and 250 μl (0.5 mmol) of aqueous 2N sodium hydroxide solution are introduced [lacuna]. The reaction medium is stirred at room temperature for 36 hours, acidified to pH 3 with hydrochloric acid solution and extracted with ethyl acetate. The organic phase is dried over magnesium sulfate, filtered and evaporated. 80 mg (46%) of the desired product, with a melting point of 117° C., are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06927228B2
Source datasetuspto-grants-2005_08
ORD IDord-c01c3dc7a2fc489284bcfc413f9b679d
Source noteuspto-grants-2005_08