HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 178527812, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Carbon Disulfide | HCID 6348 | — |
| Reactant | N4-(2-methylpropyl)quinoline-3,4-diamine | HCID 11298872 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | HCID 178527812 | HCID 178527812 | — |
Reaction Steps
N4-(2-methylpropyl)quinoline-3,4-diamine (5.4 g, 25 mmol) was combined with carbon disulfide (9 mL, 150 mmol) and ethanol (55 mL) and then heated at reflux on a steam bath for 2 hours. The resulting precipitate was isolated by filtration, washed with ethanol and then air dried to provide 4.4 g of crude product. A portion (1 g) was dissolved in hot dilute sodium hydroxide and then reprecipitated with acetic acid. The precipitate was isolated by filtration while still hot, washed with hexane and then air dried to provide thiazolo[4,5-c]quinoline-2-thiol as a solid, m.p. 282-284° C. Analysis: Calculated for C10H6N2S2: % C, 55.02; % H, 2.77; % N, 12.83: Found: % C, 54.96; % H, 2.69; % N, 12.74.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06809203B2 |
| Source dataset | uspto-grants-2004_10 |
| ORD ID | ord-96907897567b4c6eafa0dfe5b42b0a14 |
| Source note | uspto-grants-2004_10 |