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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2241171Generated: November 3, 2026

Pyridine → HCID 135927746, compound

https://huagongshe.com/reaction/2241171

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant2-Ethylhexyl chloroformateHCID 62783—
Reactant3-(5-chloro-2-methoxy-benzenesulfonylamino)-N-[4-(N-hydroxycarbamimidoyl)-phenyl]-benzamideHCID 178490725—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
ProductHCID 135927746HCID 13592774676.5%

Reaction Conditions

Temperature0 °C

Reaction Steps

A solution of 3-(5-chloro-2-methoxy-benzenesulfonylamino)-N-[4-(N-hydroxycarbamimidoyl)-phenyl]-benzamide (145 mg, 0.30 mmol) in dimethylformamide (2.0 ml) was treated with pyridine (26 mg, 1.08 equiv.) and cooled to 0° C. Chloroformic acid 2-ethylhexyl ester (59 mg, 0.30 mmol, 1 equiv.) in DMF (0.1 ml) was added dropwise. The mixture was stirred at 0° C. for 30 min, then diluted with water and extracted with ethyl acetate. The combined organic phases were dried over sodium sulfate and evaporated. The residue was suspended in xylene and the mixture was stirred at 100° C. for 1 h and then at 145° C. for 1 h. After cooling to room temperature, the precipitated solid was filtered, washing with xylene, and dried under high vacuum to yield the title compound (115 mg, 75%) as a white solid, MS (ISP): m/e=499.0 (M−H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07723538B2
Source datasetuspto-grants-2010_05
ORD IDord-fae37e0334634b4094a9bc05c76e99a2
Source noteuspto-grants-2010_05