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HRID 29102Erstellt: 24. Oktober 2026

2-Aminopyridine → [2-(5-Bromothiophen-2-yl)-imidazo[1,2-a]pyridin-3-yl]-(1,1,3,3-tetramethyl-butyl)-amine

https://huagongshe.com/de/reaction/29102

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-AminopyridineHCID 10439—
EduktPerchloric AcidHCID 24247—
Edukt1,1,3,3-Tetramethylbutyl isocyanideHCID 26725—
Edukt5-Bromothiophene-2-carbaldehydeHCID 78428—
LösungsmittelDichloromethaneHCID 6344—
Produkt[2-(5-Bromothiophen-2-yl)-imidazo[1,2-a]pyridin-3-yl]-(1,1,3,3-tetramethyl-butyl)-amineHCID 6931791371%

Reaktionsschritte

235 mg (2.5 mmol) of 2-aminopyridine were dissolved together with 0.42 ml (2.5 mmol) of 1,1,3,3-tetramethyl-butylisonitrile and 0.27 ml (2.5 mmol) of 5-bromothiophene-2-carbaldehyde in DCM (5 ml). After addition of perchloric acid (0.25 ml), the mixture was stirred at RT for 5 d. Washing was then performed with a sat. aq. sodium carbonate solution and a sat. aq. common salt solution. The organic phase was dried over magnesium sulfate, filtered and evaporated under a vacuum. After carrying out column chromatography (EA/DIPE/DCM 2:2:1) with the group, 724 mg (1.7 mmol, 71% of theoretical) of [2-(5-bromothiophen-2-yl)-imidazo[1,2-a]pyridin-3-yl]-(1,1,3,3-tetramethyl-butyl)-amine were obtained.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07420056B2
Quelldatensatzuspto-grants-2008_09
ORD IDord-5240d8b45e85487baca690c674fe436e
Quellennotizuspto-grants-2008_09