Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Tripropylamine | HCID 7616 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Methoxybenzylamine | HCID 75452 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 13853845 | HCID 13853845 | — |
| Product | HCID 13853899 | HCID 13853899 | — |
Reaction Steps
A mixture comprising 2.2 g of 4-methoxybenzylamine, 0.30 g of 4-methyl-5-chloro-2-i-propyl-3(2H)pyridazinone, 1.34 g of sodium hydrogencarbonate, 0.23 g of potassium carbonate and 5 ml of tri-n-propylamine, was heated at 150° C. for 18 hours. The reaction mixture was acidified with a 10% hydrochloric acid aqueous solution, and extracted with 60 ml of benzene. The benzene layer was washed with water, and dried over anhydrous sodium sulfate, and then the solvent was distilled off to obtain an oily substance. This substance was crystallized from 5 ml of ethyl ether to obtain 40 mg of the above identified compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05098900 |
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| Source dataset | uspto-grants-1992_03 |
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| ORD ID | ord-99f1c15da5034abab4866b56829a1836 |
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| Source note | uspto-grants-1992_03 |
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