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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1506559Generated: October 31, 2026

HCID 67169668, compound → HCID 67171061, compound

https://huagongshe.com/reaction/1506559

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 67169668HCID 67169668—
SolventHydrochloric AcidHCID 313—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 67171061HCID 6717106199.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

Methyl 2-hydroxy-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)propanoate (Preparation 134C, isomer 1, 85 mg, 0.175 mmol) was dissolved in 4 N hydrochloric acid in dioxane (1 mL). The reaction mixture stirred at 60° C. for 48 h before it was concentrated to yield 2-hydroxy-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)propanoic acid (80 mg, 0.17 mmol, 97% yield): LC/MS M+1=472.03. Isomer 2: Methyl 2-hydroxy-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)propanoate (Preparation 134C, isomer 2, 83 mg, 0.171 mmol) was dissolved in 4 N hydrochloric acid in dioxane (1 mL). The reaction mixture was stirred at 60° C. for 48 h before it was concentrated to yield 2-hydroxy-2-(3-(5-phenyl-4-(trifluoromethyl)isoxazol-3-yl)-4,5-dihydronaphtho[1,2-c]isoxazol-7-yl)propanoic acid (80 mg, 0.17 mmol, 99% yield): LC/MS M+1=472.03.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09216972B2
Source datasetuspto-grants-2015_12
ORD IDord-21ff996a78db4e7d80e0832abb28a8c2
Source noteuspto-grants-2015_12