HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16028Erstellt: 25. Oktober 2026
Diisopropylethylamine → 5-Bromo-N*3*-quinazolin-6-ylmethyl-pyrazine-2,3-diamine
https://huagongshe.com/reaction/16028
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2-Amino-3,5-dibromopyrazine | HCID 620004 | — |
| Edukt | 6-Quinazolinemethanamine | HCID 24820551 | — |
| Lösungsmittel | 1-Butanol | HCID 263 | — |
| Produkt | 5-Bromo-N*3*-quinazolin-6-ylmethyl-pyrazine-2,3-diamine | HCID 59341927 | 42% |
Reaktionsschritte
To the solution of C-quinazolin-6-yl-methylamine (1.2 g, 7.916 mmol) and 2.06 gram of 3,5-dibromo-pyrazin-2-ylamine (2.06 g, 7.916 mmol) in n-BuOH (18 mL) was added diisopropylethylamine (7.0 mL, 40 mmol) at room temperature. The reaction mixture was heated up to 120° C. for two days under nitrogen. The reaction was cooled down, n-BuOH is evaporated directly via rotavapor, followed by purification via a silica gel column to get 5-Bromo-N*3*-quinazolin-6-ylmethyl-pyrazine-2,3-diamine (1.02 g, yield 42%).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07732604B2 |
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| Quelldatensatz | uspto-grants-2010_06 |
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| ORD ID | ord-aeec7fdd72984952946b785f5861ffd7 |
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| Quellennotiz | uspto-grants-2010_06 |
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