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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1172426Generated: November 3, 2026

Trifluoroacetic acid → Methyl 6-amino-4-bromopyridine-2-carboxylate

https://huagongshe.com/reaction/1172426

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantMethyl 4-bromo-6-[(tert-butoxycarbonyl)amino]pyridine-2-carboxylateHCID 25067269—
SolventChloroformHCID 6212—
ProductMethyl 6-amino-4-bromopyridine-2-carboxylateHCID 29919299—

Reaction Steps

7.23 g of methyl 4-bromo-6-t-butoxycarbonylamino-pyridine-2-carboxylate was dissolved in 30 ml of chloroform, and then 15 ml of trifluoroacetic acid was added thereto, followed by stirring at room temperature for 1 hour. After concentrating the reaction mixture, the residue was dissolved in ethyl acetate and washed with saturated sodium bicarbonate and brine. The organic layer was dried over anhydrous magnesium sulfate, filtered, and then concentrated in vacuo. The residue was purified by a silica gel column chromatography (eluent: chloroform to chloroform/methanol=20/1) to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07834018B2
Source datasetuspto-grants-2010_11
ORD IDord-3befec2ecfa449af81857082339b92c6
Source noteuspto-grants-2010_11