HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Malonate → HCID 19104906, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Malonate | HCID 7761 | — |
| Reactant | HCID 19104933 | HCID 19104933 | — |
| Reactant | HCID 19104966 | HCID 19104966 | — |
| Product | HCID 19104906 | HCID 19104906 | — |
Reaction Steps
In a manner analogous to Example 1, by chlorinating 6-phenyl-4-propyl-3(2H)-pyridazinone [Chim. Ther. 6, 109 (1971)] there is obtained 3-chloro-6-phenyl-4-propylpyridazine, MS: 232 (M)+, which is converted by hydrazinolysis into 3-hydrazino-6-phenyl-4-propylpyridazine, MS: 228 (M)+. Subsequent ring condensation with diethyl malonate to ethyl 6-phenyl-8-propyl-s-triazolo[4,3-b]pyridazine-3-acetate, MS: 324 (M)+, followed by basic saponification gives the above acid as a solid, MS: 252 (M-CO2)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05278161 |
| Source dataset | uspto-grants-1994_01 |
| ORD ID | ord-bc46ff81396e475496fbc2f86aa94451 |
| Source note | uspto-grants-1994_01 |