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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 492739Generated: October 29, 2026

Hydrochloric Acid → 4-(4-Benzyloxycarbonylamino-3-fluorophenyl)pyridine-2-carboxylic acid

https://huagongshe.com/reaction/492739

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantMethyl 4-(4-benzyloxycarbonylamino-3-fluorophenyl)pyridine-2-carboxylateHCID 23153492—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventDimethylformamideHCID 6228—
SolventHexaneHCID 8058—
Product4-(4-Benzyloxycarbonylamino-3-fluorophenyl)pyridine-2-carboxylic acidHCID 2315337386.1%

Reaction Steps

Methyl 4-(4-benzyloxycarbonylamino-3-fluorophenyl)pyridine-2-carboxylate (1.02 g) was dissolved in a mixed solvent of ethanol (25 ml), methanol (50 ml) and N,N-dimethylformamide (7.5 ml), and then water (7.5 ml) was added. Lithium hydroxide monohydrate (185 mg) was added thereto at room temperature while stirring, followed by stirring at room temperature for 1.5 hrs. To the reaction mixture was added 1 N HCl (30 ml), followed by concentrating under a reduced pressure. To the resultant residue was added a mixed solvent of ethyl acetate (100 ml) and tetrahydrofuran (100 ml) to partition. The organic layer was washed with brine (50 ml×3), and dried over anhydrous sodium sulfate. The solvent was evaporated to give a solid, which was then suspended in a mixed solvent of diethyl ether (20 ml) and hexane (20 ml), filtered, and dried under aeration to provide the titled compound (846 mg, 86.1%) as a pale brown solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07531532B2
Source datasetuspto-grants-2009_05
ORD IDord-39687eda882b47ec8d8fd89b425a8429
Source noteuspto-grants-2009_05