HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 7-(3-Thienyl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | Ethyl 7-(3-thienyl)pyrazolo[1,5-a]pyrimidine-3-carboxylate | HCID 11818144 | — |
| Solvent | Water ethanol | HCID 19096565 | — |
| Product | 7-(3-Thienyl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid | HCID 21163069 | — |
Reaction Steps
A mixture of 0.05 mole of ethyl 7-(3-thienyl)pyrazolo[1,5-a]pyrimidine-3-carboxylate and 0.20 mole of potassium hydroxide in 50 ml. of ethanol-water is heated at reflux temperature for 4 hours. The mixture is acidified with concentrated hydrochloric acid and concentrated to give 7-(3-thienyl)pyrazolo[1,5-a]pyrimidine-3-carboxylic acid. The preceding compound in tetrahydrofuran is added dropwise to a solution of 0.10 mole of diborane in tetrahydrofuran chilled in an ice bath. After stirring for 2 hours the bath is removed and the mixture allowed to stand 6 hours at room temperature. The mixture is poured into ice to give the product of the example.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04281000 |
| Source dataset | uspto-grants-1981_07 |
| ORD ID | ord-c6d8bc888b464ffea19276e28f12d264 |
| Source note | uspto-grants-1981_07 |