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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2116661Generated: November 2, 2026

Potassium Hydroxide → HCID 86760732, compound

https://huagongshe.com/reaction/2116661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium HydroxideHCID 14797—
Reactant7-Bromo-4-(pyridin-3-yl)-2H-1-benzopyran-2-oneHCID 23370236—
ReactantHCID 178458805HCID 178458805—
SolventMethanolHCID 887—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 86760732HCID 86760732—

Reaction Conditions

Temperature120 °C

Reaction Steps

KOH (0.223 g, 3.97 mmol) was added to a solution of (2R)-1,1,1-trifluoro-2-(2-mercapto-1,3-thiazol-5-yl)butan-2-ol (0.966 g, 3.97 mmol) in dry MeOH. When a solution was obtained, the reaction mixture was concentrated to dryness. Dry toluene was then added and the mixture was concentrated to dryness again. The residue was dissolved with 7-bromo-4-pyridin-3-yl-2H-chromen-2-one (1.0 g, 3.31 mmol) in NMP, and the resulting mixture was stirred at 120° C. for 16 h. Once cooled, the mixture was directly applied onto a column of silica gel and chromatographed (acetone/toluene; 5:95 to 15:85), affording the title compound. 1H NMR (400 MHz, CDCl3): δ 8.81 (dd,1H), 8.72 (dd, 1H), 7.82 (dt, 1H), 7.78 (s, 1H), 7.51-7.59 (m, 2H), 7.33-7.40 (m, 2H), 6.42 (s, 1H), 2.88 (br s, 1H), 2.12 (q, 2H), 0.99 (t, 3H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07439260B2
Source datasetuspto-grants-2008_10
ORD IDord-2e40798ca1194e008a5d0ed2827612fa
Source noteuspto-grants-2008_10