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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 439307생성일: 2026년 10월 24일

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

https://huagongshe.com/ko/reaction/439307

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물D-Isoglutamine benzyl ester hydrochlorideHCID 22802678—
반응물N-(7-oxododecanoyl)-L-alanineHCID 54199880—
용매BenzeneHCID 241—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-(7-oxododecanoyl)-L-alanyl-D-isoglutamine benzyl esterHCID 22860847—

반응 조건

온도0 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05514654
출처 데이터셋uspto-grants-1996_05
ORD IDord-3e434807956948878cfe5375017dd202
출처 메모uspto-grants-1996_05