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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2186659생성일: 2026년 10월 27일

1,2-Dichloroethane → (1S,2S)-2-[4-(4-methoxyphenyl)butyryl]amino-3-morpholino-1-phenyl-1-propanol

https://huagongshe.com/reaction/2186659

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물TriethylamineHCID 8471—
반응물4-(4-Methoxyphenyl)butyric acidHCID 78280—
반응물(1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanolHCID 10513992—
용매DichloromethaneHCID 6344—
생성물(1S,2S)-2-[4-(4-methoxyphenyl)butyryl]amino-3-morpholino-1-phenyl-1-propanolHCID 6982147866.5%

반응 단계

Methylene chloride (10 ml), 4-(4-methoxyphenyl)butanoic acid (388.0 mg, 2.0 mmol), triethylamine (0.70 ml, 5.0 mmol) and EDC (580 mg, 3.0 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:ethanol=20:1) to obtain the title compound (549 mg, yield 66%) as colorless oil.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06407064B2
출처 데이터셋uspto-grants-2002_06
ORD IDord-b04c55622f534f38b9fb8bc490f9daf4
출처 메모uspto-grants-2002_06