HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 650011Generated: October 30, 2026
Triethylamine → 2-(N,N-dimethylaminomethyl)thieno[2,3-b][1,5]benzoxazepin-4(5H)-one
https://huagongshe.com/reaction/650011
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methanesulfonyl chloride | HCID 31297 | — |
| Reactant | 2-hydroxymethylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one | HCID 18422152 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-(N,N-dimethylaminomethyl)thieno[2,3-b][1,5]benzoxazepin-4(5H)-one | HCID 18422185 | 45.1% |
Reaction Steps
2-Hydroxymethylthieno[2,3-b][1,5]benzoxazepin-4(5H)-one (1.0 g) was dissolved in methylene chloride (10 ml) and triethylamine (450 mg) and methanesulfonyl chloride (500 mg) were added. The mixture was stirred at room temperature for 15 minutes and the solvent was evaporated under reduced pressure. Thereto was added 2M dimethylamine/methanol and the mixture was stirred at room temperature for 14 hours. The solvent was evaporated under reduced pressure and chloroform was added to the residue. After washing with water, the aqueous layer was extracted twice with chloroform. The organic layer was dried over sodium sulfate and the solvent was evaporated under reduced pressure. The residue was purified by silica gel column chromatography (ethyl acetate) to give 2-(N,N-dimethylaminomethyl)thieno[2,3-b][1,5]benzoxazepin-4(5H)-one (500 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06271225B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-83cc4ed654904113bc2078676f1c05d8 |
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| Source note | uspto-grants-2001_08 |
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