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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452832Generated: October 30, 2026

(2,5-Difluorophenyl)boronic acid → 3-(2,5-Difluorophenyl)-5-(5-methyl-1,3,4-oxadiazol-2-yl)furo[3,2-b]pyridine

https://huagongshe.com/reaction/452832

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2,5-Difluorophenyl)boronic acidHCID 2734335—
Reactant3-Bromo-5-(5-methyl-1,3,4-oxadiazol-2-yl)furo[3,2-b]pyridineHCID 68663099—
Product3-(2,5-Difluorophenyl)-5-(5-methyl-1,3,4-oxadiazol-2-yl)furo[3,2-b]pyridineHCID 6866410943%

Reaction Steps

In the same manner as in Example 132 and using 3-bromo-5-(5-methyl-1,3,4-oxadiazol-2-yl)furo[3,2-b]pyridine instead of 2-(3-bromo-1-benzofuran-5-yl)-5-methyl-1,3,4-oxadiazole, using (2,5-difluorophenyl)boronic acid instead of (4-fluorophenyl)boronic acid, and using [1,1′-bis(diphenylphosphino)ferrocene]palladium(II) chloride dichloromethane complex instead of tetrakis(triphenylphosphine)palladium(0), the title compound (yield 43%) was obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-d8a17456381a4020aa07b62976e46c87
Source noteuspto-grants-2013_07