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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 349822Generated: October 30, 2026

Hydrochloric Acid → (2R,4R)-2-Aminomethyl-4-(2,4-difluoro-benzyl)-hexanoic Acid

https://huagongshe.com/reaction/349822

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1,4-DioxaneHCID 31275—
Reactant2-tert-Butyl-5-[2-(2,4-difluoro-benzyl)-butyl]-3-methyl-4-oxo-tetrahydro-pyrimidine-1-carboxylic Acid Methyl EsterHCID 69268151—
Product(2R,4R)-2-Aminomethyl-4-(2,4-difluoro-benzyl)-hexanoic AcidHCID 6927066424%

Reaction Conditions

Temperature110 °C

Reaction Steps

A flask was charged with 0.5 g (1.2 mmol) of 2-tert-butyl-5-[2-(2,4-difluoro-benzyl)-butyl]-3-methyl-4-oxo-tetrahydro-pyrimidine-1-carboxylic acid methyl ester, 20 mL of dioxane, and 20 mL of conc. HCl solution. The mixture was stirred and heated at 110° C. for 4 days. The solvents were removed under reduced pressure. The residue was taken up in 20 mL of water and 4 drops of conc. HCl solution. The aqueous layer was washed with dichloromethane. The aqueous layer was collected and the water was removed under reduced pressure. The residue was treated with 2 mL of triethylamine, and the excess triethylamine was removed under reduced pressure. The remaining solid was purified by column chromatography (1:8:27 NH4OH, MeOH, dichloromethane eluent). The resulting white solid was washed with acetonitrile and dried under vacuum. This gave 80 mg (24% yield) of the titled compound as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07179934B2
Source datasetuspto-grants-2007_02
ORD IDord-ab933cef777242a2af271b15faaeb201
Source noteuspto-grants-2007_02