HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2296433Erstellt: 25. Oktober 2026
Pyridine → 4-Amino-6-(3,3-dimethylbutyramido)quinazoline
https://huagongshe.com/reaction/2296433
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Pyridine | HCID 1049 | — |
| Edukt | Tripropylamine | HCID 7616 | — |
| Edukt | 3,3-Dimethylbutanoyl chloride | HCID 81514 | — |
| Edukt | 4,6-Diaminoquinazoline hydrochloride | HCID 20266086 | — |
| Lösungsmittel | Methanol | HCID 887 | — |
| Lösungsmittel | Chloroform | HCID 6212 | — |
| Lösungsmittel | Chloroform methanol | HCID 21584188 | — |
| Produkt | 4-Amino-6-(3,3-dimethylbutyramido)quinazoline | HCID 13060460 | 64,7% |
Reaktionsschritte
To a mixture of 4,6-diaminoquinazoline hydrochloride (10.0 g), tripropylamine (17.61 g) and dry pyridine (100 ml) was added dropwise during 35 minutes 3,3-dimethylbutyryl chloride (10.34 g) under ice-cooling. The reaction mixture was stirred for 2 hours at the same temperature. To the resultant mixture was added ice-water. The mixture was stirred for 5 minutes and then concentrated under reduced pressure. To the residue was added water and sodium hydrogen carbonate (13.0 g) little by little to give precipitates, which were separated by filtration, washed with water and dried. Thus obtained crude crystals were dissolved in a mixture of chloroform and methanol under heating. After insoluble materials were removed by filtration, the filtrate was concentrated under reduced pressure to give a residue, which was suspended in 5% methanol-chloroform solution (70 ml). After stirring under heating, the suspension was filtered to give crystalline 4-amino-6-(3,3-dimethylbutyramido)quinazoline (8.5 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US04429126 |
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| Quelldatensatz | uspto-grants-1984_01 |
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| ORD ID | ord-1db8f0f1b6f04044b8d10eba5b4e152d |
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| Quellennotiz | uspto-grants-1984_01 |
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