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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2428202Generated: October 25, 2026

Hydrochloric Acid → 6-[3-(2-Chloro-3,6-difluoro-phenyl)-isoxazol-5-ylmethoxy]-5',6'-dihydro-2'H-[3,4']bipyridinyl-1',3'-dicarboxylic Acid 1'-tert-butyl Ester

https://huagongshe.com/reaction/2428202

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
Reactant6-[3-(2-Chloro-3,6-difluoro-phenyl)-isoxazol-5-ylmethoxy]-5',6'-dihydro-2'H-[3,4']bipyridinyl-1',3'-dicarboxylic Acid 1'-tert-butyl Ester 3'-methyl EsterHCID 67148902—
SolventTetrahydrofuranHCID 8028—
Product6-[3-(2-Chloro-3,6-difluoro-phenyl)-isoxazol-5-ylmethoxy]-5',6'-dihydro-2'H-[3,4']bipyridinyl-1',3'-dicarboxylic Acid 1'-tert-butyl EsterHCID 67148901—

Reaction Conditions

Temperature70 °C

Reaction Steps

A mixture of compound C8 (1.00 g, 1.78 mmol) and aq. 1M LiOH (7.00 mL, 7.00 mmol) in THF (7.00 mL) was stirred overnight at 70° C. Aq. 1M HCl was added until a pH=4 was reached. The mixture was extracted with EtOAc (3×). The combined org. extracts were dried over MgSO4, filtered, and the solvents were removed under reduced pressure. Drying the residue under high vacuum yielded the title compound mixed with 6-[3-(2-chloro-3,6-difluoro-phenyl)-isoxazol-5-ylmethoxy]-3′,6′-dihydro-2′H-[3,4′]bipyridinyl-1′,3′-dicarboxylic acid 1′-tert-butyl ester (976 mg, quantitative yield) that was used further without purification. LC-MS: tR=1.06 min; ES+: 548.30.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07968720B2
Source datasetuspto-grants-2011_06
ORD IDord-22ac679b4db84469b33fef7cc8b3c796
Source noteuspto-grants-2011_06