HuagongsheHuagongshe Chemistry Print Report · For research reference only
2,5-Dihydroxybenzoic acid → HCID 12582680, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2,5-Dihydroxybenzoic acid | HCID 3469 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | HCID 20441591 | HCID 20441591 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 12582680 | HCID 12582680 | — |
Reaction Steps
10.3 g of 3-chloro-6-(2,3-dimethylbenzoyl)-5,6,7,8-tetrahydropyrido[4,3-c]pyridazine and 50 cc of hydrazine hydrate in 80 cc of dioxane are heated in an oil bath of 80°. After a reaction time of 60 hours, the mixture is concentrated in a vacuum, the oily residue is divided between 250 cc of chloroform and 150 cc of water, and after concentrating the chloroform phase, the resulting oily crude base is reacted with gentisic acid as described in Example 10. The gentisinate of the title compound has a M.P. of 176°-179° (decomp.) after recrystallization from 150 cc of methanol and 100 cc of water.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US03954754 |
| Source dataset | uspto-grants-1976_05 |
| ORD ID | ord-7eef489bab3f4e819e58b47c626f4d13 |
| Source note | uspto-grants-1976_05 |