HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloro-N,N-dimethylethylamine → HCID 70490372, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloro-N,N-dimethylethylamine | HCID 7901 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | 2-[(2,4-Dichlorophenyl)methylidene]-2H-1,4-benzothiazin-3(4H)-one | HCID 54249637 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | HCID 70490372 | HCID 70490372 | — |
Reaction Steps
2-(2,4-Dichlorophenylmethylidene)-2H-1,4-benzothiazine-3(4H)-one (3.0 g) in methyl ethyl ketone (10 ml) was treated with sodium hydroxide (0.98 g) at 80° C. for 30 minutes. The reaction mixture was cooled to room temperature and added with dimethylaminoethyl chloride (1.7 g), refluxed for 3 hours and cooled to 30° C. The organic layer was washed with 20 ml of water two times, dried and evaporated under reduced pressure. The residue was dissolved in 20 ml of isopropyl alcohol and added with 0.9 ml of conc. HCl. The resulted precipitates were filtered and recrystallized from 30 ml of isopropyl alcohol to give 2-(2,4-Dichlorophenylmethylidene)-4-(2-dimethylaminoethyl)-2H-1,4-benzothiazine hydrochloride as yellow crystals. m.p. 238° to 242° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04490292 |
| Source dataset | uspto-grants-1984_12 |
| ORD ID | ord-3d912fb0f9144e58a7e18e4a07edb791 |
| Source note | uspto-grants-1984_12 |