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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256171Generated: October 31, 2026

Pyridine → HCID 67312003, compound

https://huagongshe.com/reaction/1256171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant6-Aminobenzo(c)(1,2)oxaborol-1(3H)-olHCID 3770187—
ReactantHCID 86655241HCID 86655241—
SolventAcetonitrileHCID 6342—
ProductHCID 67312003HCID 6731200391.2%

Reaction Steps

To a stirred solution of 2-((5-propyl-1,3,4-oxadiazol-2-yl)methyl)-4-(2,2,2-trifluoroacetamido)benzene-1-sulfonyl chloride (430 mg, 1.05 mmol) and 6-aminobenzo[c][1,2]oxaborol-1(3H)-ol (234 mg, 1.57 mmol) in 5 mL of ACN was added pyridine (253 uL, 3.13 mmol) dropwise. The reaction mixture was stirred at room temperature for 16 hours. After the mixture was concentrated, the residue was extracted with ethyl acetate and washed with water, 1N HCl and brine. The organic layer was dried over Na2SO4 and concentrated to give the desired compound as a yellow solid (410 mg, yield 75%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-1fd6c2dbfae540d5a93b377c9302f0bd
Source noteuspto-grants-2013_06