참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 12-Bromododecanoic Acid | HCID 175468 | — |
| 반응물 | Calcium Chloride | HCID 5284359 | — |
| 촉매 | Tetrabutylammonium Chloride | HCID 70681 | — |
| 용매 | Acetonitrile | HCID 6342 | — |
| 생성물 | 12-Chloro-dodecanoic acid | HCID 381109 | — |
반응 단계
To 12-bromododecanoic acid (1 g) dissolved in acetonitrile (50 ml) was added calcium chloride (2 g) and tetra-n-butylammonium chloride (1.2 g), and the mixture was heated under reflux for 4 hours. The reaction mixture was filtered, concentrated and distributed into ethyl acetate-water, and the ethyl acetate layer was dried over anhydrous sodium sulfate to give 12-chlorododecanoic acid. After a 280 mg portion of 12-chlorododecanoic acid thus obtained, para-nitrophenol (167 mg) and N,N'-dicyclohexylcarbodiimide (245 mg) in N,N-dimethylformamide (DMF) was stirred for 12 hours, precipitates were removed by filtration and DMF was removed by distillation to give an active ester. To the active ester of 12-chlorododecanoic acid dissolved in DMF were added 6-(4'-N-glycyl-spicaminyl-amino)purine hydrochloride (456 mg) and triethylamine (1.2 ml ), and the mixture was stirred for 12 hours. The reaction mixture was concentrated and subjected to chromatography on a silica gel column with eluent systems of chloroform-methanol (from 7:1 to 5:1) to give SPK132 in the yield of mg.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05461036 |
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| 출처 데이터셋 | uspto-grants-1995_10 |
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| ORD ID | ord-33ca184a83ca4e71846276d2b3bde25d |
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| 출처 메모 | uspto-grants-1995_10 |
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