HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 14181068, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 1,2,3,4-Tetrahydro-1-naphthylamine | HCID 18066 | — |
| Reactant | 1,1-Dioxido-2-(4-bromobutyl)-1,2-benzisothiazol-3(2H)-one | HCID 10781774 | — |
| Reactant | 8-methoxy-N-propyl-1,2,3,4-tetrahydronaphthalen-2-amine | HCID 12741417 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 14181068 | HCID 14181068 | 25% |
Reaction Steps
1.9 g (6.0 mmol) of 2-(4-bromobutyl -1,2-benzisothiazol-3(2H)-one 1,1-dioxide were added dropwise to the solution of 1.3 g (6.0 mmol) of 8-methoxy-2-propylamino-1,2,3,4-tetrahydronaphthalene and 1.3 g (12 mmol) of triethylamine in 15 ml of dimethylformamide. After stirring for 15 hours at room temperature, a spatula tip of sodium iodide was added, and the mixture was heated to 60° C. After 4 hours at this temperature, 0.4 g of the above aminotetralin and 0.3 g of triethylamine were added. Chromatography on silica gel (toluene/ethyl acetate gradients) of the crude product, obtained after removal of the solvent in vacuo, yielded 0.70 g (25%) of the title compound as a yellowish oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05153225 |
| Source dataset | uspto-grants-1992_10 |
| ORD ID | ord-a529d44b872446ce840fe4ced52eb77a |
| Source note | uspto-grants-1992_10 |