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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1894857Generated: November 1, 2026

Pyridine → HCID 68632088, compound

https://huagongshe.com/reaction/1894857

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantSulfamideHCID 82267—
ReactantN-[1-(Aminomethyl)cyclohexyl]anilineHCID 16227755—
ProductHCID 68632088HCID 6863208850%

Reaction Steps

105 mg (1.09 mmol) of sulfamide are added to a solution of 200 mg of (1-aminomethylcyclohexyl)phenylamine (obtained in Example 2b) in 5 ml of pyridine. The medium is stirred at room temperature for 24 h and then at reflux for 2 h. At room temperature, the medium is evaporated and taken up with ethyl acetate and washed with water. The organic phases are collected and dried over sodium sulfate. The solvents are evaporated. The residue is chromatographed on silica gel (ethyl acetate/heptane). 130 mg of N-(1-aminomethylcyclohexyl)-N-phenylmethanesulfonamide are obtained in the form of a yellow solid. Yield=50%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08513307B2
Source datasetuspto-grants-2013_08
ORD IDord-f129d005be1341bfbd6f141e1daed259
Source noteuspto-grants-2013_08