HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → HCID 68451882, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 5-(Methylsulfanyl)-1H-indole | HCID 13019589 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Reactant | HCID 59383129 | HCID 59383129 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 68451882 | HCID 68451882 | — |
Reaction Steps
Under a nitrogen atmosphere 500 mg (2.6 mmol) 5-(methylsulphanyl)-indole (Yang et al., Heterocycles, 1992, vol. 34, No. 6, page 1169-1175) are dissolved in 6 ml DMF and combined with 357 mg (3.2 mmol) potassium-tert-butoxide with stirring and cooling with ice. Then the mixture is stirred for 10 minutes at 0° C. 768 mg (2.9 mmol) N-tert-butoxycarbonyl-4,4-dimethyl-[1,2,3]oxathiazinane-2,2-dioxide (Component XI) are added. The mixture is then stirred for three hours at ambient temperature. Then the reaction solution is poured onto water and hydrochloric acid (1.2 mmol) and extracted with ethyl acetate. The organic phases are combined, dried on sodium sulphate and freed from the solvent in vacuo.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754756B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-3c0f46da622946f4be16837de259dbb8 |
| Source note | uspto-grants-2010_07 |