HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → Pyrazolo(1,5-a)pyridine-3-carboxamide, N,N-dimethyl-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Pyrazolo[1,5-a]pyridine-3-carbonyl chloride | HCID 2795463 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Pyrazolo(1,5-a)pyridine-3-carboxamide, N,N-dimethyl- | HCID 20240341 | — |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
A solution of dimethylamine in ethanol (35% w/v; 300 ml) was added to dichloromethane (1100 ml) and the resulting solution was stirred at 0° C. and treated slowly with a solution of pyrazolo[1,5-a]pyridine-3-carbonyl chloride (61.0 g) in dry dichloromethane (1100 ml). When the addition was complete, the mixture was allowed to warm up to room temperature and stand at room temperature overnight. The mixture was then washed twice with water and the organic solution was then dried over sodium sulphate and evaporated under reduced pressure. The resulting brown oil was recrystallised from cyclohexane, to give 3-(N,N-dimethylcarbamoyl)pyrazolo[1,5-a]pyridine (42.0 g), m.p. 86°-87° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04604400 |
| Source dataset | uspto-grants-1986_08 |
| ORD ID | ord-bcecaf4fc5984c37b89eb04df6ee1bae |
| Source note | uspto-grants-1986_08 |