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HRID 273810作成日:2026年10月27日

Hydrochloric Acid → 6-[[2-(5-Hydroxy-1H-indol-3-yl)ethyl]amino]-N-phenylheptanamide, monohydrochloride hydrate

https://huagongshe.com/reaction/273810

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Serotonin HydrochlorideHCID 160436—
反応物Sodium BicarbonateHCID 516892—
反応物Sodium cyanoborohydrideHCID 5003444—
反応物N-phenyl-6-oxo-heptanamideHCID 19422086—
溶媒EthanolHCID 702—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
生成物6-[[2-(5-Hydroxy-1H-indol-3-yl)ethyl]amino]-N-phenylheptanamide, monohydrochloride hydrateHCID 131717787176.4%

反応手順

Serotonin hydrochloride (1.000 g) and N-phenyl-6-oxo-heptanamide (1.289 g) were stirred in methanol (47 mL) under a nitrogen atmosphere and treated with sodium cyanoborohydride (0.444 g), excluding light from the reaction. After 4 d at ca. 23° C., a solution of sodium bicarbonate (1.00 g) in water (25 mL) was added. One hour later, the reaction was diluted with water (75 mL) and extracted with 1:4 2-propanol:dichloromethane (3×75 mL). The combined extracts were dried (Na2SO4), filtered, and concentrated in vacuo to a foaming oil which was chromatographed using 5:20:80 triethylamine:ethanol:ethyl acetate, isolating the component with an Rf of 0.3. The resulting oil was twice reconcentrated in vacuo from ethanol (100 mL) and then redissolved in ethanol (100 mL). This solution was treated with 1:9 concentrated hydrochloric acid: ethanol (6 mL), concentrated in vacuo reconcentrated from ethanol (100 mL) to an oil, and the oil placed under vacuum to yield the title compound as a solid (1.80 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05387604
出典データセットuspto-grants-1995_02
ORD IDord-77e8716395f14d96a5690461ff37d335
出典メモuspto-grants-1995_02