반응식
[CH3:1][C:2]1[C:13](=[O:14])[C:6]2[N:7]3[CH2:12][CH2:11][CH2:10][C:8]3=[N:9][C:5]=2[C:4](=[O:15])[CH:3]=1.[CH3:16][NH:17][CH3:18].CCCCCC.[K+].[Br-]>CN(C=O)C.C(Cl)(Cl)Cl.C(Cl)(Cl)Cl.CO>[CH3:16][N:17]([CH3:18])[C:3]1[C:4](=[O:15])[C:5]2[N:9]=[C:8]3[CH2:10][CH2:11][CH2:12][N:7]3[C:6]=2[C:13](=[O:14])[C:2]=1[CH3:1]참가 물질
반응물 4
생성물 1
시약·촉매·용매 3
실험 절차
To a solution of 50 mg (0.24 mmol) of 26 in 3 mL of dry DMF, chilled to 0° C., was added an excess of methanolic dimethylamine. After the addition, the reaction mixture was stirred at room temperature for about 30 min and then the solvent was evaporated in vacuo. The residue was chromatographed on silica gel employing chloroform as the eluant. The blue-colored 27 was obtained in 42 mg (71%) yield. An analytical sample was prepared by dissolving the residue in a small amount of chloroform, adding hexane, and then chilling the mixture overnight in the refrigerator: mp 158° C. dec; TLC (chloroform/methanol[90:10]), Rf =0.56, IR(KBr pellet) 1675, 1659, 1623, 1524, 1314, 1067 cm-1 ; 1H NMR (CDCl3) δ4.16 (2 H, t, J~7 Hz, C(1) methylene), 3.04 (6 H, s, dimethylamino), 2.87 (2 H, t, J~7 Hz, C(3) methylene), 2.64 (2 H, quintet, J~7 Hz, C(2) methylene); 1.93 (3 H, s, 7-methyl); mass spectrum (EI mode) m/z 245 (P+), 230 (P+ -CH3), 217 (P+ -CO). Anal. Calcd for C13H15N3O2.0.25: C, 62.50; H, 6.15; N, 16.82. Found: C, 62.78; H, 6.32; N, 16.64.
후처리
- additionAfter the addition
- customthe solvent was evaporated in vacuo
- customThe residue was chromatographed on silica gel
- customThe blue-colored 27 was obtained in 42 mg (71%)
- customyield
- customAn analytical sample was prepared
- temperaturechilling the mixture overnight in the refrigerator
출처 및 근거
- ORD 기록
- ord-049ccdb15aaf4163924d80045ee0f16c
- 출처 데이터셋
- uspto-grants-1991_05
- 특허 번호
- US05015742
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