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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2061861Generated: November 2, 2026

(R)-(-)-2-Amino-1-propanol → (R)-ethyl 1-(1-hydroxypropan-2-yl)-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylate

https://huagongshe.com/reaction/2061861

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(R)-(-)-2-Amino-1-propanolHCID 80308—
Reactant(Z)-ethyl 3-(dimethylamino)-2-(2-fluoro-5-iodobenzoyl)acrylateHCID 70809441—
SolventTetrahydrofuranHCID 8028—
Product(R)-ethyl 1-(1-hydroxypropan-2-yl)-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylateHCID 5941601543.4%

Reaction Conditions

Temperature60 °C

Reaction Steps

To a solution of ethyl 3-(dimethylamino)-2-(2-fluoro-5-iodobenzoyl)acrylate (Intermediate 24, 1 g, 2.56 mmol) dissolved in THF (10 mL) was added (R)-2-aminopropan -1-ol (300 mg, 2.56 mmol). The reaction mixture was stirred at 60° C. for 2 h. The reaction mixture was concentrated under reduced pressure, and the resulting residue was suspended in DMF (10 mL). Potassium carbonate was added (1.06 g, 7.67 mmol, 3 equiv.), and the reaction mixture was stirred at 70° C. for 18 h. The reaction mixture was cooled down to room temperature and quenched with 1 N HCl. The precipitate that formed was collected by filtration, washed with water and hexanes to provide (R)-ethyl 1-(1-hydroxypropan-2-yl)-6-iodo-4-oxo-1,4-dihydroquinoline-3-carboxylate (446 mg, 39%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08283361B2
Source datasetuspto-grants-2012_10
ORD IDord-501bc739298d4c70a83e5f7c4c30538a
Source noteuspto-grants-2012_10