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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 246741Erstellt: 26. Oktober 2026

Trityl chloride → 2-bromo-N-tert-butyl-5-trityl-5H-pyrrolo[3,2-b]pyrazine-7-carboxamide

https://huagongshe.com/reaction/246741

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTrityl chlorideHCID 6456—
EduktTriethylamineHCID 8471—
Edukt2-bromo-N-tert-butyl-5H-pyrrolo[2,3-b]pyrazine-7-carboxamideHCID 86677995—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-bromo-N-tert-butyl-5-trityl-5H-pyrrolo[3,2-b]pyrazine-7-carboxamideHCID 8667800875,1%

Reaktionsbedingungen

Temperatur90 °C

Reaktionsschritte

A mixture of 2-bromo-N-tert-butyl-5H-pyrrolo[3,2-b]pyrazine-7-carboxamide (378 mg, 1.272 mmol), (chloromethanetriyl)tribenzene (426 mg, 1.53 mmol) and triethylamine (193 mg, 1.91 mmol) in dry DMF (20 mL) was heated to 90° C. for 16 hours. Reaction mixture was extracted with ethyl acetate (100 mL), organic phase washed with water (3×10 mL) and brine (2×10 mL), then dried over Na2SO4, filtered and concentrated. The residue was purified by column chromatography (silica gel, 200-300 mesh, eluting with EtOAc: petroleum ether=1:15) to afford 2-bromo-N-tert-butyl-5-trityl-5H-pyrrolo[3,2-b]pyrazine-7-carboxamide (515 mg, 75%) as a white solid. 1H NMR (300 MHz, CDCl3): δ 8.29 (s, 1H), 8.01 (s, 1H), 7.29-7.26 (m, 10H), 7.13-7.11 (m, 5H), 1.51 (s, 9H). LCMS: (M+H)+=539.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08658646B2
Quelldatensatzuspto-grants-2014_02
ORD IDord-595919652e764edead8ea0c3aa3c0dba
Quellennotizuspto-grants-2014_02