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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1465947Generated: November 2, 2026

Phosphorus oxybromide → HCID 86607512, compound

https://huagongshe.com/reaction/1465947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxybromideHCID 24613—
ReactantHCID 178450839HCID 178450839—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
SolventSodium BicarbonateHCID 516892—
ProductHCID 86607512HCID 8660751255.9%

Reaction Conditions

Temperature120 °C

Reaction Steps

3-(4-Fluoro-phenyl)-4,7-dihydroxy-thieno[3,2-c]pyridine-6-carboxylic acid butyl ester (77.9 mg, 0.216 mmol), example 30-f, was suspended in 1.1 mL of anhydrous toluene. Phosphorous oxybromide (0.155 g, 0.539 mmol) was added, and the reaction mixture was heated at 120° C. for 20 min. using a CEM microwave reactor (CEM, Matthews, N.C.). The reaction mixture was diluted with ethyl acetate, and saturated sodium bicarbonate solution was then added. The biphasic mixture was stirred for 15 min. and separated to isolate the organic fraction. The organic fraction was washed with brine, dried over anhydrous sodium sulfate, and concentrated. The crude product was purified by column chromatography eluting from silica gel with dichloromethane to produce 51.2 mg of the title compound. MS: (−) m/z 422.1, 424.1 (M−1, 79Br/81Br).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09000006B2
Source datasetuspto-grants-2015_04
ORD IDord-2db67f3e60e5470b80009482f0088860
Source noteuspto-grants-2015_04