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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2170905Generated: October 30, 2026

Triisopropyl borate → HCID 68288695, compound

https://huagongshe.com/reaction/2170905

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
ReactantDichloromethane methanolHCID 21226129—
ReactantHCID 49790728HCID 49790728—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 68288695HCID 6828869581.7%

Reaction Conditions

Temperature-78 °C

Reaction Steps

6-bromo-2-(furan-2-yl)-N-(pyridin-3-yl)quinoline-4-carboxamide (0.4 g, prepared as described above for compound 1) was dissolved in THF (15 ml) in a round-bottomed flask under argon atmosphere. The solution was cooled to −78° C., then n-BuLi (15% in hexanes, 1.0 ml, 1.5 eq) was added dropwise. The reaction was maintained at this temperature for 45 minutes, at which time triisopropylborate (0.376 g, 2.0 eq.) was added dropwise. The reaction was allowed to warm to RT and stirred for an additional 3 hours. The completion of the reaction was monitored on TLC using methanol:dichloromethane (1:9) as a mobile phase. After completion of the reaction, the reaction mixture was quenched with saturated NH4Cl solution (10 ml), then was extracted with ethyl acetate (2*10 ml) which was discarded. The aqueous layer was added Conc.HCl to adjust pH up to 6-7. The solid was precipitated which further was filtered on Buckner funnel and washed with water (10 ml). The solid was dried to obtain (2-(furan-2-yl)-4-(pyridin-3-ylcarbamoyl)quinolin-6-yl)boronic acid (0.300 g) which was used as such in next step.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09051305B2
Source datasetuspto-grants-2015_06
ORD IDord-1cfdb52339744d62aab775559d7e86aa
Source noteuspto-grants-2015_06