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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1919641Generated: October 30, 2026

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

https://huagongshe.com/reaction/1919641

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 numberUS08168651B2
Source datasetuspto-grants-2012_05
ORD IDord-2090ed9bb0b543aba7a03117a0b336ed
Source noteuspto-grants-2012_05