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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 452835Generated: October 25, 2026

1-Benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole → 3-(1-benzyl-1H-pyrazol-4-yl)-5-(5-methyl-1,3,4-oxadiazol-2-yl)furo[3,2-b]pyridine

https://huagongshe.com/reaction/452835

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-Benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2734771—
Reactant3-Bromo-5-(5-methyl-1,3,4-oxadiazol-2-yl)furo[3,2-b]pyridineHCID 68663099—
Product3-(1-benzyl-1H-pyrazol-4-yl)-5-(5-methyl-1,3,4-oxadiazol-2-yl)furo[3,2-b]pyridineHCID 6866379668%

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 1-benzyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole 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 68%) was obtained as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08492378B2
Source datasetuspto-grants-2013_07
ORD IDord-099c9730de404dbf9a8b878d0331b1cf
Source noteuspto-grants-2013_07