Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
1,2-Dichloroethane → (1S,2S)-2-[4-(4-methoxyphenyl)butyryl]amino-3-morpholino-1-phenyl-1-propanol
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 1,2-Dichloroethane | HCID 11 | — |
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4-(4-Methoxyphenyl)butyric acid | HCID 78280 | — |
| 반응물 | (1S,2S)-2-amino-3-morpholino-1-phenyl-1-propanol | HCID 10513992 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (1S,2S)-2-[4-(4-methoxyphenyl)butyryl]amino-3-morpholino-1-phenyl-1-propanol | HCID 69821478 | 66.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US06407064B2 |
| 출처 데이터셋 | uspto-grants-2002_06 |
| ORD ID | ord-b04c55622f534f38b9fb8bc490f9daf4 |
| 출처 메모 | uspto-grants-2002_06 |