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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 730832생성일: 2026년 10월 25일

Diisopropylethylamine → Methyl N-{[(9H-fluoren-9-ylmethyl)oxy]carbonyl}-D-norleucylglycinate

https://huagongshe.com/reaction/730832

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Glycine methyl ester hydrochlorideHCID 122755—
반응물CarbodiimideHCID 160435—
반응물HOAtHCID 181649—
반응물(2R)-2-({[(9H-fluoren-9-yl)methoxy]carbonyl}amino)hexanoic acidHCID 2756111—
용매DichloromethaneHCID 6344—
생성물Methyl N-{[(9H-fluoren-9-ylmethyl)oxy]carbonyl}-D-norleucylglycinateHCID 67401200—

반응 단계

A mixture of fmoc-D-Nle-OH (10 g, 28.3 mmol, Novabiochem) and PS-carbodiimide (33 g, 42.45 mmol, 1.28 mmol/g, Argonaut Technologies Inc.) in dichloromethane (250 mL) was stirred at room temperature for 0.5 h. Then, glycine methyl ester hydrochloride (5.3 g, 42.45 mmol, Aldrich), HOAt (3.8 g, 28.3 mmol, Perseptive Biosystems) and diisopropylethylamine (16 mL, 84.9 mmol, Aldrich) were added and the mixture was stirred at room temperature for 16 h. The mixture was filtered and the resin was washed with dichloromethane (2×70 mL). The filtrate was concentrated in vacuo and the residue was purified by column chromatography, eluting with EtOAc/hexane (1:2) to give the title compound as a yellow solid. MS (ESI, positive ion) m/z: 425 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07582761B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-82221a597aeb4b0184ba9efcc11632d3
출처 메모uspto-grants-2009_09