HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 645703Erstellt: 25. Oktober 2026
1H-Indazol-6-amine → 2-chloro-N-(1H-indazol-6-yl)-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine
https://huagongshe.com/reaction/645703
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | 1H-Indazol-6-amine | HCID 81423 | — |
| Edukt | Diisopropylethylamine | HCID 81531 | — |
| Edukt | 2,4-dichloro-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine | HCID 57990293 | — |
| Lösungsmittel | 1-Butanol | HCID 263 | — |
| Produkt | 2-chloro-N-(1H-indazol-6-yl)-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine | HCID 86628040 | 60,9% |
Reaktionsschritte
To a mixture of 2,4-dichloro-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidine (1.5 g, 3.2 mmol) in n-butyl alcohol (12 mL) was added 6-aminoindazole (0.47 g, 3.52 mol) and DIPEA (0.86 mL, 4.80 mmol). After heating at 45° C. for 15 h, the mixture was cooled to room temperature, and the resulting precipitates were collected by filtration to give 2-chloro-N-(1H-indazol-6-yl)-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (1.1 g).
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US07705004B2 |
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| Quelldatensatz | uspto-grants-2010_04 |
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| ORD ID | ord-a93399419ff6477086166b7e7980ff53 |
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| Quellennotiz | uspto-grants-2010_04 |
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