HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Hydroxide → 2-Ethylthiazolo[4,5-c]quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | Propionic anhydride | HCID 31263 | — |
| Reactant | 3-Aminoquinoline-4-thiol | HCID 178507990 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Product | 2-Ethylthiazolo[4,5-c]quinoline | HCID 15027904 | 90% |
Reaction Steps
A mixture of 17.62 g (0.1 mole) of 3-amino-4-mercapto-quinoline and 85 ml of propionic anhydride is first slowly heated to boiling and then refluxed for one hour and a half. The reaction mixture is added dropwise to 800 ml of 1% aqueous hydrochloric acid under vigorous stirring. The homogenous solution is made alkaline to pH 10 by adding sodium hydroxide solution and extracted three times with 200 ml of benzene each. The benzene solution is evaporated. Thus 19.26 g of 2-ethylthiazolo[4,5-c]quinoline are obtained, yield 90%, m.p.: 48°-49° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04904669 |
| Source dataset | uspto-grants-1990_02 |
| ORD ID | ord-23e264946d404672b45bc35b0d549f8a |
| Source note | uspto-grants-1990_02 |