HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethanol → HCID 19081373, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 4-Pyridinemethanamine | HCID 77317 | — |
| Reactant | HCID 19081414 | HCID 19081414 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 19081373 | HCID 19081373 | 88.9% |
Reaction Steps
Into a 30 ml of ethanol solution of 2.1 g of 2-tert-butyl-5-chloro-4-cyanopyridazin-3-(2H)-one and 1.0 g of triethylamine, 1.1 g of 4-picolylamine was dropwise added under cooling with ice over a period of 5 minutes. Then, the mixture was stirred at room temperature for two hours and then concentrated. The mixture was extracted with ethyl acetate, and the extract was washed twice with a saturated sodium chloride aqueous solution and then dried. Ethyl acetate was distilled off under reduced pressure, and the residue thereby obtained was subjected to column chromatography. Using an eluent (ethyl acetate:methanol=20:1), 2.5 g of the desired product (Compound No. 21) having a melting point of from 174 to 175° C., was obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05763439 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-0c7fd0657cca45789a553115c49303b7 |
| Source note | uspto-grants-1998_06 |