Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 968519생성일: 2026년 10월 26일
Dicyclohexylcarbodiimide → 2-{[(3r)-4-(4-Toluenesulfonyl)thiomorpholine-3-carbonyl]amino}-3-phenyl-propionic acid benzyl ester
https://huagongshe.com/reaction/968519
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 반응물 | L-phenylalanine benzyl ester p-toluenesulfonate | HCID 12636207 | — |
| 반응물 | (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid | HCID 69415969 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | 2-{[(3r)-4-(4-Toluenesulfonyl)thiomorpholine-3-carbonyl]amino}-3-phenyl-propionic acid benzyl ester | HCID 69414241 | 74.3% |
반응 단계
0.602 g (2 mmol) of (3R)-4-(4-toluenesulfonyl)thiomorpholine-3-carboxylic acid, 0.939 g (2.2 mmol) of L-phenylalanine benzyl ester p-toluenesulfonic acid salt, 0.454 g (2.2 mmol) of DCC and 0.224 g (2 mmol) of DMAP were dissolved in 30 mL of CH2Cl2, 0.4 ml (2.7 mmol) of TEA was added. The mixture was stirred for 24 h at room temperature. The solid was filtrated and the solvent was evaporated. The residual was dissolved in a suitable amount of ethyl acetate (20 ml) and then the mixture was filtered to remove insoluble substance. The ethyl acetate was added to 60 ml and then the liquid was washed with 10% NaHCO3 solution, saturated NaCl solution and dried over Na2SO4. After the drying agent was removed and part of ethyl acetate was evaporated, the crude product was purified by flash column chromatography (eluent: CH2Cl2:CH3Cl=1:1) to obtain the product as a glassy solid (0.80 g).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07304057B2 |
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| 출처 데이터셋 | uspto-grants-2007_12 |
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| ORD ID | ord-d0398c28489646e8a39a048de5a6ed8b |
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| 출처 메모 | uspto-grants-2007_12 |
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