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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174905Generated: November 1, 2026

Hydrochloric Acid → 2-Bromo-4-oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylic acid

https://huagongshe.com/reaction/2174905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantLithium HydroxideHCID 3939—
ReactantMethanol tetrahydrofuran waterHCID 21892291—
ReactantMethyl 2-bromo-4-oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylateHCID 57500654—
SolventWaterHCID 962—
Product2-Bromo-4-oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylic acidHCID 5750065513%

Reaction Steps

Methyl 2-bromo-4-oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylate (1.0 eq, 17 mg, 0.050 mmol) was suspended in a 1:1:1 mixture of MeOH/THF/water (0.6 ml). LiOH (39 mg) was added and the mixture stirred at room temperature for one hour. Water and 6N HCl was added and the resulting precipitate was filtered. The material was purified by preparative HPLC. Genevac evaporation provided 2-bromo-4-oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylic acid as a solid (2.1 mg, 13% yield). LCMS (ES): >95% pure, m/z 324 [M]+, 326[M+2]+; 1H NMR (DMSO-d6, 400 MHz) δ 7.75 (s, 1H), 7.75 (dd, J=1.6, J=8.0, 1H), 7.90 (d, J=8.4, 1H), 8.03 (d, J=1.6, 1H), 12.06 (s, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062043B2
Source datasetuspto-grants-2015_06
ORD IDord-48ce46b7b9ab4c55acd2e074ba8afea0
Source noteuspto-grants-2015_06