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HRID 1907作成日:2026年10月25日

1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochloride → (R)-alpha-[(2-t-Butoxycarbonylamino-2-methyl-1-oxopropyl)amino]-1H-indole-3-propanoic acid, benzyl ester

https://huagongshe.com/reaction/1907

反応式

関与物質

役割名称HCID仕込み量
反応物1,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 2723939—
反応物N-((1,1-dimethylethoxy)carbonyl)-2-methyl-alanineHCID 2733845—
反応物1-Hydroxybenzotriazole hydrateHCID 2796029—
反応物D-Tryptophan benzyl esterHCID 6995075—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物(R)-alpha-[(2-t-Butoxycarbonylamino-2-methyl-1-oxopropyl)amino]-1H-indole-3-propanoic acid, benzyl esterHCID 86752261—

反応手順

Crude D-tryptophan benzyl ester (1.0 g, 3.40 mmol), 1-hydroxybenztriazole hydrate (0.63 g, 4.1 mmol) and t-butoxycarbonyl-α-methylalanine (0.84 g, 4.11 mmol) were stirred together at room temperature in chloroform (20 mL). 1-(3-Dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (980 mg, 5.11 mmol) was added to this mixture in a single portion. The reaction mixture was stirred at room temperature for 4 hours and worked up by pouring into water (50 mL). The chloroform layer was separated and washed with 5% aqueous citric acid solution (25 mL) and 5% aqueous sodium bicarbonate solution (25 mL). The chloroform layer was dried over magnesium sulfate, filtered and evaporated under vacuum to afford a thick oily foam. Chromatography on silica gel using ethyl acetate/hexanes (2:3 v/v) afforded a yellow foam (0.822 g 50%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05726319
出典データセットuspto-grants-1998_03
ORD IDord-d5d90023934e416fa9241ef7aa4c808a
出典メモuspto-grants-1998_03