Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Dichloromethane | HCID 6344 | — |
| Edukt | Butyl chloroformate | HCID 61140 | — |
| Edukt | HCID 178507852 | HCID 178507852 | — |
| Lösungsmittel | Triethylamine | HCID 8471 | — |
| Produkt | HCID 178452819 | HCID 178452819 | — |
Reaktionsschritte
20 G. of 2,4-diamino-6-[3,6-dihydro-1(2H)-pyridyl]pyrimidine-3-oxide are mixed with 250 ml. of methylene chloride and 35 ml. of triethylamine, stirred and cooled to 5° C. The mixture is treated with 45 ml. of chloroformic acid butyl ester and stirred at room temperature for 6 hours. The mixture obtained is washed with water, extracted with methylene chloride and evaporated under reduced pressure. The residue is recrystallized from ethanol, there being obtained dibutyl 6-[3,6-dihydro-1(2H)-pyridyl]-2,4-pyrimidine-dicarbamate-3-oxide, having a melting point of 131°-132° C.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patentnummer | US04150132 |
|---|
| Quelldatensatz | uspto-grants-1979_04 |
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| ORD ID | ord-aaf95424dd714d558075c4f775f387bd |
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| Quellennotiz | uspto-grants-1979_04 |
|---|