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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 924371Generated: November 1, 2026

Acetic Acid → 3-Amino-7-bromoquinoline-2-carboxylic acid

https://huagongshe.com/reaction/924371

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTetrahydrofuranHCID 8028—
ReactantLithium hydroxide, monohydrateHCID 168937—
ReactantEthyl 3-amino-7-bromoquinoline-2-carboxylateHCID 56965769—
SolventWaterHCID 962—
Product3-Amino-7-bromoquinoline-2-carboxylic acidHCID 7355487080.8%

Reaction Conditions

Temperature50 °C

Reaction Steps

To a mixture of ethyl 3-amino-7-bromoquinoline-2-carboxylate (Ark Pharm, 113.9 mg, 0.3859 mmol) and lithium hydroxide monohydrate (82.8 mg, 1.97 mmol), THF (2.50 mL) was added, followed by water (0.50 mL). The resulting mixture was stirred at 50° C. for 2 h. The reaction mixture was then cooled to room temperature and water (25 mL) was then added, followed by AcOH (245.9 mg, 4.095 mmol) to adjust the pH to 5. The mixture was extracted with EtOAc (3×25 mL). The combined organic extract was washed with brine (50 mL), then dried over Na2SO4, and concentrated to yield a yellow solid (83.3 mg). The crude product was used directly in the next step without further purification. LCMS calc. for C10H8BrN2O2(M+H)+: m/z=267.0. found 267.0.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09278950B2
Source datasetuspto-grants-2016_03
ORD IDord-8a5d4fab190f416587de20e4fb3a380b
Source noteuspto-grants-2016_03