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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 16686Erstellt: 23. Oktober 2026

Sodium Bicarbonate → HCID 178483849, Verbindung

https://huagongshe.com/de/reaction/16686

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktSodium BicarbonateHCID 516892—
Edukt1-Amino-3,3-diethoxypropaneHCID 521029—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt3-t-Butoxycarbonyl-aminopropanalHCID 19434596—
EduktHCID 178484811HCID 178484811—
LösungsmittelChloroformHCID 6212—
LösungsmittelTriethylamineHCID 8471—
ProduktHCID 178483849HCID 178483849—

Reaktionsschritte

N-(5-Chloropyridin-2-yl)-3-({[trans-4-(methylamino)-cyclohexyl]carbonyl}amino)furo[3,2-b]pyridine-2-carboxamide trihydrochloride (300 mg) obtained in Example 119 is suspended in chloroform (7 ml). To the suspension are added 3-t-butoxycarbonyl-aminopropanal (208 mg), which can be prepared from 3-aminopropionaldehyde diethyl acetal in two steps according to the method described in a literature (Synthesis, 1994, 37) and triethylamine (334 μl) under ice-cooling, and the mixture is stirred for a few minutes. After addition of sodium triacetoxy borohydride (190 mg), the reaction solution is warmed to room temperature and stirred for 2 hours. To the reaction solution is poured saturated aqueous sodium hydrogen carbonate solution under ice-cooling, and the mixture is extracted with chloroform. The organic layer is washed successively with water and saturated brine, dried over sodium sulfate, and the solvent is evaporated under reduced pressure. The resulting residue is purified by NH-silica gel column chromatography (eluent: ethyl acetate followed by ethyl acetate/methanol=20/1) to give the title compound (291 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737161B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-ac3e7add2f9e43c8bde1cac7e0d86eba
Quellennotizuspto-grants-2010_06