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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2174903Generated: October 31, 2026

Methanol → 7-(hydroxymethyl)thieno[3,2-c]quinolin-4(5H)-one

https://huagongshe.com/reaction/2174903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantWaterHCID 962—
ReactantAluminium lithium hydrideHCID 21226445—
Reactant4-Oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylic acidHCID 50941753—
SolventDichloromethaneHCID 6344—
Solvent1,4-DioxaneHCID 31275—
Product7-(hydroxymethyl)thieno[3,2-c]quinolin-4(5H)-oneHCID 5094175434%

Reaction Conditions

Temperature100 °C

Reaction Steps

4-oxo-4,5-dihydrothieno[3,2-c]quinoline-7-carboxylic acid (1.0 eq, 38 mg, 0.155 mmol) was suspended in dioxane (1 ml). LiAlH4 (7.0 eq, 40 mg, 1.05 mmol) was added and the mixture stirred at 100° C. for 45 nm. Water was added, then MeOH and CH2Cl2. The solid salts were filtered off and washed with MeOH and CH2Cl2. After evaporation of the volatiles in vacuo, the material was dissolved in a mixture of NMP, MeOH and water and was purified by preparative HPLC. Genevac evaporation afforded 7-(hydroxymethyl)thieno[3,2-c]quinolin-4(5H)-one as an off-white solid (12 mg, 34%). LCMS (ES): 95% pure, m/z 232 [M+1]+; 1H NMR (DMSO-d6, 400 MHz) δ 4.56 (s, 2H), 7.15 (d, J=7.6, 1H), 7.39 (br s, 1H), 7.55 (d, J=5.2, 1H), 7.73 (d, J=5.2, 1H), 7.76 (d, J=8.0, 1H), 11.73 (s, 1H) ppm.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09062043B2
Source datasetuspto-grants-2015_06
ORD IDord-33dcb117b3a44cc18b85f2a519715afa
Source noteuspto-grants-2015_06