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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2387214Generated: November 1, 2026

Triisopropyl borate → HCID 86634553, compound

https://huagongshe.com/reaction/2387214

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriisopropyl borateHCID 21531—
ReactantN-(5-Bromo-2-chloropyridin-3-yl)benzenesulfonamideHCID 57843322—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
ProductHCID 86634553HCID 86634553—

Reaction Conditions

Temperature-78 °C

Reaction Steps

Triisopropyl borate (5.69 ml, 24.7 mmol) is added to a solution of N-(5-Bromo-2-chloro-pyridin-3-yl)-benzenesulfonamide (1 g, 2.87 mmol) in anhydrous THF (25 ml) under argon, and the resulting solution is cooled to −78° C. A 1.6 M solution of n-butyl lithium in hexanes (5.39 ml, 8.63 mmol) is added dropwise keeping the temperature below −70° C. The reaction is stirred at −78° C. for 50 minutes. The reaction is quenched with sat. aq. NaCl (20 ml) at −78° C. and then allowed to warm to room temperature and washed with EtOAc. The aqueous layer is concentrated in vacuo, and the residue is dissolved in 2.5M HCl, and the product is extracted into EtOAc, dried (MgSO4) and concentrated in vacuo to yield the title compound as a yellow oil. [M+H]+ 313.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08268834B2
Source datasetuspto-grants-2012_09
ORD IDord-400b457fb27f466eaf4a47d09abc94fc
Source noteuspto-grants-2012_09