참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Dicyclohexylcarbodiimide | HCID 10868 | — |
| 반응물 | Bendamustine | HCID 65628 | — |
| 반응물 | 1-Morpholinoethanol | HCID 3029376 | — |
| 촉매 | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | N,N'-Dicyclohexylurea | HCID 4277 | — |
반응 단계
Bendamustine free base (1.0 g, 2.79 mmol) in dichloromethane (90 ml), morpholinoethanol (0.44 ml, 3.35 mmol) and DMAP (20 mg) were added with stirring. A solution of N,N′-Dicyclohexylcarbodiimide (0.63 g, 3.05 mmol) in dichloromethane (90 ml) was added dropwise over 50 min. After 15 min, a clear reaction solution was obtained and after 70 min a precipitate of dicyclohexyl urea occurred. The reaction mixture was stirred at ambient temperature for a total time of 24 h. After concentration to half of the volume and cooling to 0° C., the precipitate was removed by filtration. Then the solution was extracted with diluted HCl (1 ml 37% HCl to 60 ml Water, 30 ml+2×15 ml portions). The aqueous phase was treated with 25% NH3 (1.6 ml, pH 7-8) and extracted with dichloromethane (20+2×10 ml). Evaporation of the combined organic solvents resulted in a crude oil (1.38 g) that was purified via column chromatography (40 g silica, 10% MeOH/dichloromethane) to afford a slightly yellowish oil (1.26 g) that crystallized after seeding. Further drying in vacuum resulted in 1.08 g (82%) of product as slightly yellowish crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08809549B2 |
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| 출처 데이터셋 | uspto-grants-2014_08 |
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| ORD ID | ord-1310d7d1bd964f098812de757199cc64 |
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| 출처 메모 | uspto-grants-2014_08 |
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