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HRID 16686作成日:2026年10月23日

Sodium Bicarbonate → HCID 178483849、化合物

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

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium BicarbonateHCID 516892—
反応物1-Amino-3,3-diethoxypropaneHCID 521029—
反応物Sodium triacetoxyborohydrideHCID 5049666—
反応物3-t-Butoxycarbonyl-aminopropanalHCID 19434596—
反応物HCID 178484811HCID 178484811—
溶媒ChloroformHCID 6212—
溶媒TriethylamineHCID 8471—
生成物HCID 178483849HCID 178483849—

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737161B2
出典データセットuspto-grants-2010_06
ORD IDord-ac3e7add2f9e43c8bde1cac7e0d86eba
出典メモuspto-grants-2010_06