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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1256163Generated: November 1, 2026

Pyridine → HCID 67173130, compound

https://huagongshe.com/reaction/1256163

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant6-Aminobenzo(c)(1,2)oxaborol-1(3H)-olHCID 3770187—
ReactantHCID 86655233HCID 86655233—
SolventAcetonitrileHCID 6342—
ProductHCID 67173130HCID 67173130—

Reaction Steps

To a stirred solution of 2-(oxazol-2-ylmethyl)-4-(2,2,2-trifluoroacetamido)benzene-1-sulfonyl chloride (450 mg, 1.2 mmol) and 6-aminobenzo[c][1,2]oxaborol-1(3H)-ol (212 mg, 1.42 mmol) in 10 mL of ACN was added pyridine (228 uL, 2.8 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 (540 mg, yield 92%). 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-bdb0d4f4eb8546c6a0c758b60442e3a7
Source noteuspto-grants-2013_06