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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1766187Generated: November 3, 2026

Triethylamine → HCID 21109929, compound

https://huagongshe.com/reaction/1766187

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethanesulfonyl chlorideHCID 31297—
ReactantHCID 21109928HCID 21109928—
SolventTetrahydrofuranHCID 8028—
ProductHCID 21109929HCID 21109929—

Reaction Steps

1.64 ml. (21 mmol) of methanesulphonyl chloride was added dropwise to a solution of 7.91 g (20 mmol) of N-(1,1-dimethylethoxycarbonyl)-N-[(2-aminophenyl)methyl]-1-(phenylmethyl)-4-piperidineamine and 3.0 ml (21 mmol) of triethylamine in 100 ml of tetrahydrofuran and the mixture was then kept for 12 hours at ambient temperature. It was then diluted with 100 ml of EE and extracted twice with 70 ml of saturated sodium hydrogen carbonate solution. The ethyl acetate phase was dried over sodium sulphate and concentrated by evaporation in vacuo. 8.7 g (92% of theoretical) of a colourless substance were obtained, Rf 0.85 (El D), which were used in the next step without any further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07230001B1
Source datasetuspto-grants-2007_06
ORD IDord-2276117a2a99496cbec32e38cdedf1cd
Source noteuspto-grants-2007_06