HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanethiol → 6-Ethylthio-2-trifluoromethylimidazo[1,2-b]pyridazin-3-ylsulfonamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanethiol | HCID 6343 | — |
| Reactant | 6-Chloro-2-(trifluoromethyl)imidazo[1,2-b]pyridazine-3-sulfonamide | HCID 23028108 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 6-Ethylthio-2-trifluoromethylimidazo[1,2-b]pyridazin-3-ylsulfonamide | HCID 23028118 | — |
Reaction Steps
6-Chloro-2-trifluoromethylimidazo[1,2-b]pyridazin-3-ylsulfonamide (1.00 g, 3.33 mmol) was suspended in t-butyl alcohol (20.0 ml) and stirred at room temperature, during which potassium t-butoxide (80%, 1.40 g, 9.98 mmol) and ethanethiol (0.54 ml, 7.29 mmol) were added thereto. After the mixture was heated for 4 hours under reflux, the reaction solution was left and cooled to room temperature, poured into ice-water (200 ml) and adjusted to pH 3. The precipitated crystals were filtered and washed with water to give the title compound as colorless crystals. The yield was 0.54 g (50.0%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07816526B2 |
| Source dataset | uspto-grants-2010_10 |
| ORD ID | ord-2c0ea649e952468daa7124c4237ac838 |
| Source note | uspto-grants-2010_10 |