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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Chloroethyl methyl sulfide | HCID 10965 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 19429156 | HCID 19429156 | — |
| Reactant | HCID 23646094 | HCID 23646094 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylacetamide | HCID 31374 | — |
| Product | 2-Chloro-5-[2-(methylsulfanyl)ethyl]pyrido[2,3-b][1,4]benzoxazepin-6(5H)-one | HCID 453956 | 78.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05547951 |
|---|
| Source dataset | uspto-grants-1996_08 |
|---|
| ORD ID | ord-6518c709488845f0a092026b71efb9e4 |
|---|
| Source note | uspto-grants-1996_08 |
|---|