반응식
[NH2:1][C:2]1[N:3]=[CH:4][NH:5][C:6]=1[C:7]#[N:8].[C:9]([NH2:16])(=O)[CH2:10][CH2:11][CH2:12][CH2:13][CH3:14].[CH2:17](Cl)[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1.C([O-])([O-])=O.[K+].[K+]>CN(C=O)C.O>[CH2:17]([N:3]1[CH:4]=[N:5][C:6]2[C:2]1=[N:1][C:9]([CH2:10][CH2:11][CH2:12][CH2:13][CH3:14])=[N:16][C:7]=2[NH2:8])[C:18]1[CH:23]=[CH:22][CH:21]=[CH:20][CH:19]=1참가 물질
반응 조건
- 온도
- 210 °C
실험 절차
A mixture of 4-amino-5-cyanoimidazole (1.09 g, 11 mmol) and hexaneamide (4.39 g, 38 mmol) was heated at 210° C. for 15 h under N2 atmosphere. After cooling, the residue was dissolved in a mixture of DMF (200 ml) and water (50 ml). Benzyl chloride (3 ml) and K2CO3 (3 g) was added to the mixture, and heated at 70° C. for 6 h. Solvent was evaporated under vacuum, the residue was extracted by CH2Cl2. The resulting organic layer was evaporated under vacuum. 9-benzyl-2-pentyladenine was obtained by the purification of the residue by column chromatography (CH2Cl2 :MeOH=100:1-50:1). Bromine (2 ml) was added to the mixture of 9-benzyl-2-hexyladenine and NaOAc (5 g) in ACOH (40 ml) within an ice bath, and the mixture was heated at 70° C. for 6 h. Solvent was evaporated under vacuum, the residue was extracted by EtOAc. The resulting organic layer was evaporated under vacuum, 9-benzyl-8-bromo-2-pentyladenine was obtained by the purification of the residue by column chromatography (CH2Cl2 :MeOH=100:1). A mixture of 9-benzyl-8-bromo-2-pentyladenine and conc.HCl (20 ml) was refluxed for 6 h. After cooling, aqueous NH3 was added to neutralize and crystallize the product (pH=8), and the desired compound was collected by filtration (0.25 g, Yield: 8%).
후처리
- temperatureAfter cooling
- temperatureheated at 70° C. for 6 h
- customSolvent was evaporated under vacuum
- extractionthe residue was extracted by CH2Cl2
- customThe resulting organic layer was evaporated under vacuum
출처 및 근거
- ORD 기록
- ord-8979a20551f64a62b127c1a10ecde08c
- 출처 데이터셋
- uspto-grants-2000_02
- 특허 번호
- US06028076
연결된 노트
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