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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113415Generated: November 2, 2026

Lithium Hydroxide → 4-Amino-3-chloro-6-ethyl-5-fluoropyridine-2-carboxylic acid

https://huagongshe.com/reaction/2113415

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium HydroxideHCID 3939—
ReactantMethyl 4-amino-3-chloro-6-ethyl-5-fluoropyridine-2-carboxylateHCID 67026614—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
Product4-Amino-3-chloro-6-ethyl-5-fluoropyridine-2-carboxylic acidHCID 6702660978.5%

Reaction Steps

A solution of lithium hydroxide (0.49 g, 11.73 mmol) in water (25 mL) was added to a solution of methyl 4-amino-3-chloro-6-ethyl-5-fluoropyridine-2-carboxylate (1.36 g, 5.86 mmol) in tetrahydrofuran (25 mL). The mixture was vigorously stirred at room temperature overnight and was then concentrated to half volume. After adding water the reaction mixture was washed once with ethyl acetate to remove unreacted starting material. The aqueous layer was then acidified to pH<3 with 1N HCl, concentrated and the residue partitioned between tetrahydrofuran and brine. The aqueous layer was discarded and the organic layer concentrated and dried under vacuum to provide 4-amino-3-chloro-6-ethyl-5-fluoropyridine-2-carboxylic acid (1.01 g, 4.60 mmol) as a white solid, mp 144-145° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432227B2
Source datasetuspto-grants-2008_10
ORD IDord-447f19aa406c428fbf8a92b64913814b
Source noteuspto-grants-2008_10