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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 246391Erstellt: 25. Oktober 2026

Tert-Butylamine → N-tert-butyl-2-(5-methoxy-1-methyl-1H-indazol-3-yl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide

https://huagongshe.com/reaction/246391

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTert-ButylamineHCID 6385—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt2-(5-methoxy-1-methyl-1H-indazol-3-yl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acidHCID 71279852—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-tert-butyl-2-(5-methoxy-1-methyl-1H-indazol-3-yl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamideHCID 7127951389,2%

Reaktionsbedingungen

Temperatur25 °C

Reaktionsschritte

In a 16×100 mm screw cap test tube were added HATU (40.2 mg, 106 μmol.20) and 2-methylpropan-2-amine (25.8 mg, 353 μmol) then 2-(5-methoxy-1-methyl-1H-indazol-3-yl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxylic acid (40 mg, 88.2 mmol) dissolved in DMF (2.00 mL) was added to give a light yellow solution which immediately formed a white precipitated. The reaction mixture stirred at 25° C. overnight, solvents evaporated and residue purified by chromatography (spherical silica 20-45 μm, 23 g, Versaflash Supelco) eluting with 0 to 50% EtOAc in hexanes over 30 min to yield N-tert-butyl-2-(5-methoxy-1-methyl-1H-indazol-3-yl)-5-((2-(trimethylsilyl)ethoxy)methyl)-5H-pyrrolo[2,3-b]pyrazine-7-carboxamide (40 mg, 78.6 μmol, 89.2%) as an off-white solid. MS (M+H)+=509 (>90% purity); 1H NMR (CDCl3) δ: 9.11 (s, 1H), 8.32 (s, 1H), 8.20 (s, 1H), 7.85 (d, J=2.3 Hz, 1H), 7.40 (d, J=9.1 Hz, 1H), 7.20 (dd, J=9.1, 2.3 Hz, 1H), 5.72 (s, 2H), 4.18 (s, 3H), 3.92 (s, 3H), 3.54-3.64 (m, 2H), 1.58 (s, 9H), 0.90-1.01 (m, 2H), −0.03 (s, 9H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658646B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-4105c66e36d742eba285fc55f611cfbd
Quellennotizuspto-grants-2014_02