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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 369071Generated: October 28, 2026

Triethylamine → HCID 53641702, compound

https://huagongshe.com/reaction/369071

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactant2,6-Difluorobenzenesulfonyl chlorideHCID 2734271—
ReactantHCID 11000970HCID 11000970—
SolventDichloromethaneHCID 6344—
ProductHCID 53641702HCID 5364170241.4%

Reaction Steps

Triethylamine (0.62 ml) was added to a solution of (S)-4-(aminomethyl)-1-(7-chloro-1,4-benzodioxan-2-ylmethyl)piperidine (0.44 g) and 2,6-difluorobenzene-sulphonyl chloride (0.62 g) in dichloromethane (22 ml), under nitrogen, and stirred for 20 hours. The reaction was diluted with dichloromethane (100 ml), washed with water (100 ml) and brine (100 ml), dried over anhydrous magnesium sulphate and concentrated under reduced pressure to afford an orange oil. Purification by flash chromatography on silica gel eluting with a 20:1 mixture of dichloromethane and methanol gave an orange gum. Trituration with petroleum ether (b.p. 40-60° C.) yielded (S)-(-)-N-{[1-(7-chloro-1,4-benzodioxan-2-ylmethyl)-4-piperidyl]methyl}-2,6-difluorobenzenesulphonamide as an off-white solid (0.29 g); m.p. 122-124° C., [α]D22.5 -22.1° (c=1.0, CH2Cl2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06136825
Source datasetuspto-grants-2000_10
ORD IDord-e82548ecd5f34cf7b599571afb4fc9f9
Source noteuspto-grants-2000_10