HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanolamine → HCID 54397096, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanolamine | HCID 700 | — |
| Reactant | HCID 22676971 | HCID 22676971 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 54397096 | HCID 54397096 | 86% |
Reaction Steps
15 g of 7-chloro-5-methyl-3-nitropyrazolo[1,5-a]pyrimidine in 100 cc of ethanol were introduced into a 250 cc three-necked round-bottomed flask equipped with a magnetic stirrer, a thermometer and a condenser. 5 g of ethanolamine were added dropwise and the medium was refluxed for 30 minutes. After cooling to room temperature, the yellow precipitate was filtered off. This precipitate was rinsed with diisopropyl ether. After drying under vacuum over phosphorus pentoxide, 14.2 g of 7-β-hydroxyethylamino-5-methyl-3-nitropyrazolo[1,5-a]pyrimidine were obtained in the form of yellow crystals. (Yield=86%, melting point=231° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06099593 |
| Source dataset | uspto-grants-2000_08 |
| ORD ID | ord-47ba908dc58c4ca18fd193d42d60a8ef |
| Source note | uspto-grants-2000_08 |