HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2111665Erstellt: 25. Oktober 2026
Diisopropylethylamine → 5-Bromo-2-(3-methylisoxazol-5-ylmethylamino)-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidine
https://huagongshe.com/reaction/2111665
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
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| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | (3-Methyl-1,2-oxazol-5-yl)methanamine hydrochloride | HCID 45792534 | — |
| Edukt | 5-bromo-2-chloro-N-(5-methyl-1H-pyrazol-3-yl)-4-Pyrimidinamine | HCID 50993645 | — |
| Lösungsmittel | 1-Butanol | HCID 263 | — |
| Produkt | 5-Bromo-2-(3-methylisoxazol-5-ylmethylamino)-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidine | HCID 60154285 | 31% |
Reaktionsschritte
A mixture of 5-aminomethyl-3-methylisoxazole hydrochloride (890 mg, 6.0 mmol), 5-bromo-2-chloro-4-(5-methyl-1H-pyrazol-3-ylamino)pyrimidine (Method 1; 578 mg, 2.0 mmol) and N,N-diisopropylethylamine (1.4 ml, 8.0 mmol) in 1-butanol (10 ml) was heated at 120° C. for 18 hours. The mixture was allowed to cool to ambient temperature and volatiles removed by evaporation. The residue was triturated with ether and the product collected by filtration to give the titled compound (225 mg, 31%). 1H NMR (DMSO): δ 2.15 (s, 3H), 2.2 (s, 3H), 4.5 (m, 2H), 6.1 (br s, 2H), 7.6 (br s, 1H), 8.0 (br s, 2H), 12.05 (br s, 1H); MS: m/z 366.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07521453B2 |
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| Quelldatensatz | uspto-grants-2009_04 |
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| ORD ID | ord-cf5dbee485fe4d8dbb0df7bc2ba3b85d |
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| Quellennotiz | uspto-grants-2009_04 |
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