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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256173Generated: October 30, 2026

Pyridine → HCID 67174436, compound

https://huagongshe.com/reaction/1256173

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant6-Aminobenzo(c)(1,2)oxaborol-1(3H)-olHCID 3770187—
ReactantHCID 86655243HCID 86655243—
SolventAcetonitrileHCID 6342—
ProductHCID 67174436HCID 67174436—

Reaction Steps

To a stirred solution of 2-((5-methyl-1,2,4-oxadiazol-3-yl)methyl)-4-(2,2,2-trifluoroacetamido)benzene-1-sulfonyl chloride (490 mg, 1.3 mmol) and 6-aminobenzo[c][1,2]oxaborol-1(3H)-ol (627 mg, 4.21 mmol) in 10 mL of ACN was added pyridine (680 uL, 8.4 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 residue (555 mg, yield 88%). A small portion of the crude mixture was purified by prep HPLC (SunFire Prep C18 OBD 5 uM 30×50 mm column) to give the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461134B2
Source datasetuspto-grants-2013_06
ORD IDord-27c270ef52584ac8acbdc4e7c257d73b
Source noteuspto-grants-2013_06