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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1855295Generated: November 2, 2026

Lithium diisopropylamide → 7-bromo-3-chloro-1-fluoro-5H-chromeno[2,3-c]pyridin-5-one

https://huagongshe.com/reaction/1855295

Reaction equation

Participants

RoleNameHCIDCharge
ReactantLithium diisopropylamideHCID 2724682—
ReactantTetrahydrofuran heptane ethylbenzolHCID 22742125—
ReactantHCID 86640732HCID 86640732—
SolventTetrahydrofuranHCID 8028—
Product7-bromo-3-chloro-1-fluoro-5H-chromeno[2,3-c]pyridin-5-oneHCID 57475642—

Reaction Conditions

Temperature-78 °C

Reaction Steps

To a solution of 5-bromo-2-(6-chloro-2-fluoropyridin-3-yloxy)-N,N-diethylbenzamide (120 mg, 0.299 mmol) in 5 mL of dry THF at −78° C. was added dropwise lithium diisopropylamide, 2.0M heptane/THF/ethylbenzene (158 μL, 1.195 mmol) (0.6 mL of 2M solution) and the reaction was stirred at −78° C. for 3 h. The reaction was quenched at −78° C. with sat. NH4Cl and was allowed to warm up to RT. The reaction was extracted with ETOAc, dried over Na2SO4, filtered and evaporated to dryness. The crude was purified by column chromatography (1:1 hexane/DCM to 100% DCM) to give the titled compound, 7-bromo-3-chloro-1-fluoro-5H-chromeno[2,3-c]pyridin-5-one, as an offwhite solid. MS (M+1): 328.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08962859B2
Source datasetuspto-grants-2015_02
ORD IDord-292ef61033a547029fd7f788d58d8c3a
Source noteuspto-grants-2015_02