Sodium Iodide → N-{2-[(9-Benzyl-6-fluoro-9H-carbazol-4-yl)oxy]ethyl}-N,N-diethylamine

HRID 1057630노트

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HRID 1057630 반응식
[CH2:1]([N:8]1[C:20]2[CH:19]=[CH:18][CH:17]=[C:16]([OH:21])[C:15]=2[C:14]2[C:9]1=[CH:10][CH:11]=[C:12]([F:22])[CH:13]=2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.Cl.[CH2:24]([N:26]([CH2:30][CH3:31])[CH2:27][CH2:28]Cl)[CH3:25].C(=O)([O-])[O-].[K+].[K+].[I-].[Na+]>CN(C=O)C>[CH2:1]([N:8]1[C:20]2[CH:19]=[CH:18][CH:17]=[C:16]([O:21][CH2:25][CH2:24][N:26]([CH2:30][CH3:31])[CH2:27][CH3:28])[C:15]=2[C:14]2[C:9]1=[CH:10][CH:11]=[C:12]([F:22])[CH:13]=2)[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1

참가 물질

6

실험 절차

9-Benzyl-6-fluoro-9H-carbazol-4-ol (0.0587 g, 0.20 mmol), 2-diethylaminoethylchloride hydrochloride (0.0524 g, 0.30 mmol), potassium carbonate (0.0872 g, 0.63 mmol), sodium iodide (0.0062 g, 0.041 mmol) and DMF (2 mL) are heated at 85° C. for 3 h. After the mixture had cooled, it is partitioned between water and ethyl acetate. The combined organic layers are dried over magnesium sulfate and concentrated to an oil. The oil is chromatographed on silica gel (50 mL) using methanol/dichloromethane (1/99 to 3/97) to give 0.0485 g (62%) of the title compound; mp 68-69° C.; MS (ESI+) for C25H27FN2O m/z 391.3 (M+H)+; IR (drift) 2966, 1584, 1483, 1463, 1345, 1268, 1185, 1162, 1145, 1052, 799, 778, 741, 726, 713 cm−1; 1H NMR (CDCl3) δ1.14, 2.73, 3.10, 4.33, 5.48, 6.68, 6.97, 7.11, 7.21, 7.35, 8.03. Anal. Calcd for C25H27FN2O: C, 76.89; H, 6.97; N, 7.17. Found: C, 77.16; H, 7.28; N, 7.16.

후처리

  1. temperatureAfter the mixture had cooled
  2. customit is partitioned between water and ethyl acetate
  3. dry with materialThe combined organic layers are dried over magnesium sulfate
  4. concentrationconcentrated to an oil
  5. customThe oil is chromatographed on silica gel (50 mL)

출처 및 근거

ORD 기록
ord-68b74dedaeed45d79bed26e755681c4b
출처 데이터셋
uspto-grants-2003_02
특허 번호
US06514968B1

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