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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 8702Erstellt: 25. Oktober 2026

Triethylamine → N-(1-Benzyl-4-methylpiperidin-3-yl)-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine

https://huagongshe.com/reaction/8702

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt1-benzyl-N,4-dimethylpiperidin-3-amineHCID 9943889—
EduktHCID 178418725HCID 178418725—
ProduktN-(1-Benzyl-4-methylpiperidin-3-yl)-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amineHCID 1208482950%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

A solution of 4-chloropyrrolo[2,3-d]pyrimidine (2.4 grams, 15.9 mmol), prepared by the method of Davoll, J. Am. Chem. Soc., 82, 131 (1960), which is incorporated by reference in its entirety, and the product from Method A (1.7 grams, 7.95 mmol) dissolved in 2 equivalents of triethylamine was heated in a sealed tube at 100° C. for 3 days. Following cooling to room temperature and concentration under reduced pressure, the residue was purified by flash chromatography (silica; 3% methanol in dichloromethane) affording 1.3 grams (50%) of the title compound as a colorless oil. LRMS: 336.1 (M+1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07091208B2
Quelldatensatzuspto-grants-2006_08
ORD IDord-c3867a2cb80c486397e66b825750f7a8
Quellennotizuspto-grants-2006_08