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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 604367Generated: October 29, 2026

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

https://huagongshe.com/reaction/604367

Reaction equation

Participants

RoleNameHCIDCharge
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 6NHCl 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 numberUS07910600B2
Source datasetuspto-grants-2011_03
ORD IDord-5423f45479144982b7865cdf8aac3378
Source noteuspto-grants-2011_03