Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | m-Toluidine | HCID 7934 | — |
| Reactant | 4,6-Dichloroquinazoline | HCID 246024 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 20450372 | HCID 20450372 | 64.7% |
Reaction Steps
4.0 g of 4,6-dichloroquinazoline were dissolved in 50 ml of dioxan and then 2.0 g of m-toluidine were added. The mixture was then heated to reflux for 3 hours at 100° C. After completion of the reaction, the precipitated product was collected by filtration and recrystallized from ethanol to afford 3.7 g (yield 60%) of the desired Compound No. 4, in the form of pale yellow needles melting at 251°-254° C. (with decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04322420 |
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| Source dataset | uspto-grants-1982_03 |
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| ORD ID | ord-451f427be8cf418d8e46f54afe1ab6e4 |
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| Source note | uspto-grants-1982_03 |
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