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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2250356Generated: October 30, 2026

2-Fluoropyridine-3-boronic acid → HCID 15603654, compound

https://huagongshe.com/reaction/2250356

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Fluoropyridine-3-boronic acidHCID 2783270—
ReactantHCID 15603653HCID 15603653—
ReactantHCID 58772593HCID 58772593—
ProductHCID 15603654HCID 1560365442%

Reaction Steps

The title compound (41 mg, 42%) as a yellow solid was prepared from 6-chloro-7-(4-chlorophenyl)-2-((6-(trifluoromethyl)pyridin-3-yl)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one (88 mg, 0.2 mmol) and 2-fluoropyridin-3-ylboronic acid (56 mg, 0.4 mmol) according to the procedures described for 7-(4-chlorophenyl)-6-phenyl-2-((6-(trifluoromethyl)pyridin-3-yl)methyl)-[1,2,4]triazolo[4,3-b]pyridazin-3(2H)-one (Example 9). LC/MS (method A): retention time=3.38 min, (M+H)+=501. 1H NMR (CDCl3, 400 MHz): δ 8.84 (s, 1H), 8.14 (d, J=1.96 Hz, 1H), 7.97-8.01 (m, 1H), 7.68-7.76 (m, 2H), 7.46 (s, 1H), 7.34 (d,J=8.56 Hz, 2H), 7.04 (d,J=8.56 Hz, 2H), 6.89 (dd,J=8.56, 2.93 Hz, 1H), 5.34 (s, 2H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07317012B2
Source datasetuspto-grants-2008_01
ORD IDord-eefb0cadf1d0491fab04370a7faf830e
Source noteuspto-grants-2008_01