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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2186656생성일: 2026년 10월 25일

1,2-Dichloroethane → (1S,2S)-2-(5-cyclohexylcarbamoyl)pentanoylamino-3-morpholino-1-phenyl-1-propanol

https://huagongshe.com/reaction/2186656

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물MethanolHCID 887—
반응물TriethylamineHCID 8471—
반응물(1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanolHCID 10513992—
반응물6-(Cyclohexylamino)-6-oxohexanoic acidHCID 22448403—
용매DichloromethaneHCID 6344—
생성물(1S,2S)-2-(5-cyclohexylcarbamoyl)pentanoylamino-3-morpholino-1-phenyl-1-propanolHCID 6982134968%

반응 단계

A mixed solvent of methylene chloride:methanol=4:1 (10 ml), 5-cyclohexylcarbamoylpentanoic acid (546.0 mg, 2.4 mmol), triethylamine (620 μl, 4.4 mmol) and EDC (460 mg, 2.4 mmol) were added to (1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanol (472.0 mg, 2.0 mmol), followed by stirring overnight. Methylene chloride (100 ml) was added to the reaction solution. After washed with a saturated sodium hydrogen carbonate solution (50 ml), water (50 ml) and saturated brine (50 ml) successively, the organic layer was dried over sodium sulfate and filtered, and the solvent was evaporated under reduced pressure. The resulting crude product was purified by silica gel column chromatography (chloroform:methanol=10:1) to obtain the title compound (607 mg, yield 68.0%) as colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06407064B2
출처 데이터셋uspto-grants-2002_06
ORD IDord-b54169715d0048df991a09d8ca586ae2
출처 메모uspto-grants-2002_06