HuagongsheHuagongshe Chemistry Print Report · For research reference only
4H-Pyrido(2,1-a)phthalazine-1-carboxamide, 10-chloro-N,N-diethyl-4-oxo-3-phenyl- → HCID 53647567, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4H-Pyrido(2,1-a)phthalazine-1-carboxamide, 10-chloro-N,N-diethyl-4-oxo-3-phenyl- | HCID 3066689 | — |
| Reactant | Lithium borohydride | HCID 4148881 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 53647567 | HCID 53647567 | — |
Reaction Steps
2.7 g of 10-chloro-N,N-diethyl-4-oxo-3-phenyl-4H-pyrido[2,1-a]phthalazine-1-carboxamide are suspended in 65 ml of tetrahydrofuran under argon, whereupon 150 mg of lithium borohydride are added thereto, the mixture is stirred at room temperature for 4 hours, an additional 75 mg of lithium borohydride are added thereto and the mixture is stirred further until the reaction finishes. The reaction mixture is poured into 300 ml of ice-water, whereby the product crystallizes out. The crude product is chromatographed on silica gel. By recrystallization from toluene, there is obtained 10-chloro-N,N-diethyl-6,7-dihydro-4-oxo-3-phenyl-4H-pyrido[2,1-a]phthalazine-1-carboxamide of m.p. 192°-194° (toluene).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04889854 |
| Source dataset | uspto-grants-1989_12 |
| ORD ID | ord-b9a40d64ddf54b1d9783742b6953f9e7 |
| Source note | uspto-grants-1989_12 |