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HRID 1088616作成日:2026年10月27日

Triethylamine → HCID 178444652、化合物

https://huagongshe.com/reaction/1088616

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物P,P-Diphenylphosphinic azideHCID 199401—
反応物CP 84364HCID 664657—
反応物2(S)-(L-histidyl)amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptaneHCID 178444655—
溶媒DimethylformamideHCID 6228—
生成物HCID 178444652HCID 17844465268%

反応手順

To a solution of N-morpholinocarbonyl-L-phenylalanine (114 mg) and 2(S)-(L-histidyl)amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane (150 mg) in dry N,N-dimethylformamide (20 ml) which was cooled to 0° C., were added a solution of diphenyl phosphorylazide (125 mg) in dry N,N-dimethylformamide (5 ml) and triethylamine (46 mg). The mixture was stirred overnight at ambient temperature. After evaporation of the solvent, the residue was dissolved in ethyl acetate (30 ml) and the solution was washed with saturated sodium bicarbonate solution and water successively, dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified with silica gel column chromatography (2% methanol in chloroform as eluent) to give 2(S)-(N-morpholinocarbonyl-L-phenylalanyl-L-histidyl)amino-1-cyclohexyl-3(S)-hydroxy-6-methylheptane (174 mg) as an amorphous powder.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04963530
出典データセットuspto-grants-1990_10
ORD IDord-eb9f394e87734c65ab59dd17e75d7428
出典メモuspto-grants-1990_10