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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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1H-Indazol-6-amineHCID 81423—
EduktDiisopropylethylamineHCID 81531—
Edukt2,4-dichloro-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidineHCID 57990293—
Lösungsmittel1-ButanolHCID 263—
Produkt2-chloro-N-(1H-indazol-6-yl)-5-iodo-7-tosyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 8662804060,9%

Reaktionsbedingungen

Temperatur45 °C

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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07705004B2
Quelldatensatzuspto-grants-2010_04
ORD IDord-a93399419ff6477086166b7e7980ff53
Quellennotizuspto-grants-2010_04