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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 434298Generated: November 1, 2026

Triethylamine → HCID 68809404, compound

https://huagongshe.com/reaction/434298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 68809401HCID 68809401—
SolventDichloromethaneHCID 6344—
ProductHCID 68809404HCID 68809404—

Reaction Steps

To a solution of ((R)-1-(4-amino-benzyl)-2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-ethyl)-carbamic acid tert-butyl ester (1.19 g, 2.61 mmol) in dichloromethane (15 ml) cooled to 0° C. is added triethylamine (0.37 ml, 2.65 mmol) and methanesulfonylchloride (0.192 ml, 2.49mmol). The reaction mixture is allowed to warm to ambient temperature with stirring for 1 hour, then washed with water and saturated brine solution, dried over magnesium sulphate and evaporated. The crude product is purified by flash silica chromatography (ethylacetate:hexane gradient 6:4 to 1:0 elution) to afford [(R)-2-[4-(4-fluoro-benzoyl)-piperidin-1-yl]-1-(4-methanesulfonylamino-benzyl)-ethyl]-carbamic acid tert-butyl ester. [MH]+534.7.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06670379B2
Source datasetuspto-grants-2003_12
ORD IDord-0ee28b6ea0d5432181226c426ef54563
Source noteuspto-grants-2003_12