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HRID 439307作成日:2026年10月25日

Triethylamine → N-(7-oxododecanoyl)-L-alanyl-D-isoglutamine benzyl ester

https://huagongshe.com/reaction/439307

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D-Isoglutamine benzyl ester hydrochlorideHCID 22802678—
反応物N-(7-oxododecanoyl)-L-alanineHCID 54199880—
溶媒BenzeneHCID 241—
溶媒DimethylformamideHCID 6228—
溶媒Ethyl AcetateHCID 8857—
生成物N-(7-oxododecanoyl)-L-alanyl-D-isoglutamine benzyl esterHCID 22860847—

反応条件

温度0 °C

反応手順

N-(7-oxododecanoyl)-L-alanine (590 mg, 2.07 mmoles) and D-isoglutamine benzyl ester hydrochloride (565 mg, 2.07 mmoles) were dissolved in N,N-dimethylformamide (7 ml). The solution was cooled to 0° C. and diphenylphosphoryl azide (578 mg, 2.1 mmoles) and triethylamine (424 mg, 4.2 mmoles) were added thereto. The reaction mixture was stirred for 1 hour on an ice bath and for another 48 hours at room temperature. To the resulting suspension there were added benzene (5 ml) and ethyl acetate (25 ml) and it was washed successively with citric acid (0.52M; 3×5 ml), water (3×5 ml), saturated NaCl solution (3×5 ml), saturated NaHCO3 solution (3×5 ml), water (3×5 ml) and saturated NaCl solution (3×5 ml). The organic phase was dried with MgSO4 and filtered, the filtrate was evaporated and the compound was precipitated from n-hexane/diethyl ether.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05514654
出典データセットuspto-grants-1996_05
ORD IDord-3e434807956948878cfe5375017dd202
出典メモuspto-grants-1996_05