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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256169Generated: October 31, 2026

Pyridine → HCID 67174085, compound

https://huagongshe.com/reaction/1256169

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant6-Aminobenzo(c)(1,2)oxaborol-1(3H)-olHCID 3770187—
ReactantHCID 86655239HCID 86655239—
SolventAcetonitrileHCID 6342—
ProductHCID 67174085HCID 67174085112.1%

Reaction Steps

To a stirred solution of 2-((5-ethyl-1,3,4-oxadiazol-2-yl)methyl)-4-(2,2,2-trifluoroacetamido)benzene-1-sulfonyl chloride (335 mg, 0.84 mmol) and 6-aminobenzo[c][1,2]oxaborol-1(3H)-ol (125 mg, 0.84 mmol) in 5 mL of ACN was added pyridine (205 uL, 2.53 mmol) dropwise. The reaction mixture was stirred at room temperature for 3 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 (390 mg, yield 91%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-8c7c74d452034aaf98893607cdee9868
Source noteuspto-grants-2013_06