돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 439308생성일: 2026년 10월 26일

Triethylamine → N-(5-phthalimidopentanoyl)-L-alanyl-D-isoglutamine benzyl ester

https://huagongshe.com/reaction/439308

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물5-(1,3-dioxo-2,3-dihydro-1H-isoindol-2-yl)pentanoic acidHCID 1714918—
반응물benzyl L-alanyl-D-isoglutaminate hydrochlorideHCID 12873810—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물N-(5-phthalimidopentanoyl)-L-alanyl-D-isoglutamine benzyl esterHCID 22860846—

반응 조건

온도0 °C

반응 단계

L-alanyl-D-isoglutamine benzyl ester hydrochloride (548 mg, 1.6 mmoles) and 5-phthalimidopentanoic acid (400 mg, 1.6 mmoles) were dissolved in N,N-dimethylformamide (8 ml). The solution was cooled to 0° C. and diphenylphosphoryl azide (495 mg, 1.8 mmoles) and triethylamine (323 mg, 3.2 mmoles) were added thereto. The reaction mixture was stirred for 1 hour at 0° C. and for 24 hours at room temperature. The reaction mixture was diluted by ethyl acetate (40 ml) and the organic phase was washed successively with citric acid (0.52M; 3×10 ml), water (3×10 ml), saturated NaCl solution (3×10 ml), saturated NaHCO3 solution (3×10 ml), water (3×10 ml) and saturated NaCl solution (3×10 ml). The organic phase was dried with MgSO4 and filtered, the filtrate was evaporated and the product was precipitated from n-hexane/diethyl ether. The compound was filtered off and crystallized from acetone.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05514654
출처 데이터셋uspto-grants-1996_05
ORD IDord-7a25c840ab3f425a85ddf6761c65a1d6
출처 메모uspto-grants-1996_05