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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1912080Generated: October 26, 2026

Hydrogen Bromide → 4-{4-Cyclopropyl-5-[3-(2,2-dimethylpropyl)cyclobutyl]isoxazol-3-yl}-5-(2,4-dimethylphenylcarbamoyl)valeric acid

https://huagongshe.com/reaction/1912080

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrogen BromideHCID 260—
ReactantSodium AcetateHCID 517045—
ReactantMethyl 4-{4-cyclopropyl-5-[3-(2,2-dimethylpropyl)cyclobutyl]isoxazol-3-yl}-5-(2,4-dimethylphenylcarbamoyl)valerateHCID 71114790—
SolventAcetic AcidHCID 176—
Product4-{4-Cyclopropyl-5-[3-(2,2-dimethylpropyl)cyclobutyl]isoxazol-3-yl}-5-(2,4-dimethylphenylcarbamoyl)valeric acidHCID 7111479497.5%

Reaction Steps

Methyl 4-{4-cyclopropyl-5-[3-(2,2-dimethylpropyl)cyclobutyl]isoxazol-3-yl}-5-(2,4-dimethylphenylcarbamoyl)valerate (115 mg) and acetic acid (1.2 mL) were mixed. To the mixture was added 47% hydrobromic acid (0.6 mL) at 10° C. The mixture was stirred at RT and further stirred at 60° C. To the reaction mixture was added sodium acetate (492 mg) at ice temperature. The mixture was extracted with ethyl acetate. The organic layer was washed with water and brine, then dried over magnesium sulfate. The magnesium sulfate was filtered off and the filtrate was concentrated in vacuo. The resultant residue was purified by preparative chromatography (Eluent: methanol/chloroform/acetic acid=1/20/0.05) to give the title compound (109 mg). The resulting title compound was analyzed using a chiral column. The retention time of the title compound was 24.7 min., and the optical purity thereof was 94.9% ee.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604069B2
Source datasetuspto-grants-2013_12
ORD IDord-d2fa317a9ba7415dbd712524364e4de5
Source noteuspto-grants-2013_12