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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 248831Generated: October 26, 2026

Ethanethiol → 8-chloro-N-[4-(ethylthio)-2-oxobutyl]dibenz[b,f][1,4]oxazepin-10(11H)-carboxamide

https://huagongshe.com/reaction/248831

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanethiolHCID 6343—
ReactantPiperidineHCID 8082—
ReactantBenzyltrimethylammonium hydroxideHCID 66854—
Reactant8-chloro-N-(2-oxo-3-butenyl)dibenz-[b,f][1,4]oxazepin-10(11H)-carboxamideHCID 10831197—
SolventMethanolHCID 887—
SolventDichloromethaneHCID 6344—
Product8-chloro-N-[4-(ethylthio)-2-oxobutyl]dibenz[b,f][1,4]oxazepin-10(11H)-carboxamideHCID 10740032—

Reaction Steps

A solution of 8-chloro-N-(2-oxo-3-butenyl)dibenz[b,f][1,4]oxazepin-10(11H)-carboxamide (1.00 gram), ethanethiol (0.23 mL), piperidine (0.092 mL), and N-benzyltrimethylammonium hydroxide (0.092 mL) in methylene chloride (16 mL) and methanol (4 mL) was stirred at room temperature for 5 hours. The reaction was diluted with methylene chloride (100 mL), washed with 100 mL each of 1N HCl (two times), water, saturated aqueous sodium bicarbonate, and brine, dried over MgSO4, and evaporated in vacuo. The crude product was purified by flash chromatography through silica gel 60 (350 mL) using 92:8 methylene chloride: ethyl acetate to yield a colorless oil. The yield of the title compound was 0.38 gram. (32%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05212169
Source datasetuspto-grants-1993_05
ORD IDord-e3afc6be919640caa08c2ae344a25e92
Source noteuspto-grants-1993_05