Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ici 109,081 | HCID 161928 | — |
| Reactant | 2-Thiothymine | HCID 720471 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178430887 | HCID 178430887 | 14.7% |
Reaction Steps
A stirred mixture of 6-(4-aminophenyl)-5-methyl-4,5-dihydro-3(2H)-pyridazinone (3.25 g) and 5-methylthiouracil (2.5 g) was heated at 180° C. for 11/2 hours. The residual gum was dissolved in hot aqueous ethanol and the solution was evaporated. Trituration of the residue with chloroform:methanol (10:1) gave the crude product as a solid (0.78 g), m.p. 260°-270° C. The filtrate was evaporated and the residue was heated at 180° C. for one hour. Purification of the residue by column chromatography (silica gel, chloroform:methanol, 25:1) gave a further amount of product (0.73 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04962110 |
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| Source dataset | uspto-grants-1990_10 |
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| ORD ID | ord-59fd5866dd4541f0b53485c68a1045d1 |
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| Source note | uspto-grants-1990_10 |
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