Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Methyl 3-methylanthranilate | HCID 2763406 | — |
| Edukt | HCID 14155111 | HCID 14155111 | — |
| Lösungsmittel | Pyridine | HCID 1049 | — |
| Produkt | HCID 14155300 | HCID 14155300 | — |
Reaktionsschritte
Methyl 3-methylanthranilate (2.1 g, 13 mmol) was dissolved in 4 ml pyridine and 6-methyl-1,2,4-triazolo-[1,5-a]pyrimidine-2-sulfonyl chloride was added. After a mild exothermic reaction subsided the reaction mixture was stirred at 50° C. for 24 hours. The pyridine was removed by evaporation at reduced pressure and the residue was treated with in 10% aqueous sodium bicarbonate. Insoluble material was collected by filtration, washed with ether and dried to yield 2.9 (63%) of the desired product as a solid, mp 198.5°-205° C. An analytical sample was prepared by recrystallization from ethanol to yield a crystalline solid, mp 208.5°-210.5° C. IR and 1H NMR spectra were in agreement with the assigned structure.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04886883 |
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| Quelldatensatz | uspto-grants-1989_12 |
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| ORD ID | ord-ac0caadbec874f039ccb897bacfe56f8 |
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| Quellennotiz | uspto-grants-1989_12 |
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