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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 374685생성일: 2026년 10월 24일

Triethylamine → HCID 54242229, 화합물

https://huagongshe.com/ko/reaction/374685

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물CaprineHCID 21236—
반응물P,P-Diphenylphosphinic azideHCID 199401—
반응물HCID 14582181HCID 14582181—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물HCID 54242229HCID 54242229—

반응 조건

온도-15 °C

반응 단계

20.7 mg of L-N-[(2R or S)-5-ethylthio-2-(naphthylmethyl)pentanoyl]norleucine was dissolved in 0.5 ml of dry DMF. Then, 27.4 μl of triethylamine, 12.9 μl of DPPA and 20 mg of (2RS,4S,5S)-5-amino-2-ethyl-4-hydroxy-7-methyloctanoic acid isobutylamide monohydrochloride was added thereto under stirring at -15° C. The mixture was stirred at the same temperature for one hour and then at 5° C. overnight. The reaction solution was diluted with 20 ml of ethyl acetate, washed with water and with a saturated sodium chloride aqueous solution and dried over anhydrous sodium sulfate. Then, the solvent was distilled off under reduced pressure. The residue was purified by silica gel column chromatography (chloroform/methanol=50/1) to obtain 16.9 mg of (2RS,4S,5S)-5-{L-N-[(2R or S)-5-ethylthio-2-(1-naphthylmethyl)pentanoyl]norleucyl}amino-2-ethyl-4-hydroxy-7-methyloctanoic acid isobutylamide as colorless solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05481036
출처 데이터셋uspto-grants-1996_01
ORD IDord-b6084522f7014ffaa529682d1bee6a84
출처 메모uspto-grants-1996_01