Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1078205Generated: November 1, 2026

2-Chloroethyl methyl sulfide → 2-Chloro-5-[2-(methylsulfanyl)ethyl]pyrido[2,3-b][1,4]benzoxazepin-6(5H)-one

https://huagongshe.com/reaction/1078205

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Chloroethyl methyl sulfideHCID 10965—
ReactantSodium hydrideHCID 24758—
ReactantHCID 19429156HCID 19429156—
ReactantHCID 23646094HCID 23646094—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
Product2-Chloro-5-[2-(methylsulfanyl)ethyl]pyrido[2,3-b][1,4]benzoxazepin-6(5H)-oneHCID 45395678.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To as suspension of 17.0g (0.069 mole) 2-Chloropyrido[2,3-b][1,4]benzoxazepin-6(5H)-one and 150 mL of N,N-dimethylacetamide was added 9.8g of sodium hydride (50%). The mixture was warmed to 60° C. for 30 minutes. To the reaction mixture 12.2g (0.11 mole) of 2-chloroethylmethylsulfide was added dropwise. The mixture was heated to 120° C. for 4 hours, then cooled to room temperature and poured into water. The crude product was purified by column chromatography using silica gel and then recrystallized from petroleum ether/benzene to yield 17.3g (78% yield) of 2-chloro-5-(methylthioethyl)pyrido[2,3-b][1,4]benzoxazepin-6(5H)-one, m.p. 126°-128° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05547951
Source datasetuspto-grants-1996_08
ORD IDord-6518c709488845f0a092026b71efb9e4
Source noteuspto-grants-1996_08