Sodium Iodide → 8-(4-Methylpiperazin-1-yl)naphthalen-2-ol

HRID 399449

반응식

HRID 399449 반응식
[NH2:1][C:2]1[CH:3]=[CH:4][CH:5]=[C:6]2[C:11]=1[CH:10]=[C:9]([OH:12])[CH:8]=[CH:7]2.C(=O)(O)[O-].[Na+].[I-].[Na+].[CH3:20][N:21]([CH2:25][CH2:26]Cl)[CH2:22][CH2:23]Cl.Cl.[OH-].[NH4+].C1C=CC2C(=CC=CC=2O)C=1>C(#N)C.CO.C(Cl)Cl>[CH3:20][N:21]1[CH2:25][CH2:26][N:1]([C:2]2[CH:3]=[CH:4][CH:5]=[C:6]3[C:11]=2[CH:10]=[C:9]([OH:12])[CH:8]=[CH:7]3)[CH2:23][CH2:22]1

참가 물질

10

실험 절차

To a stirring solution of 8-amino-2-naphthol (3.28 g, 20 mmol, Aldrich Chem. Co.) in 100 mL of acetonitrile was added sodium bicarbonate (7.42 g, 88 mmol), sodium iodide (6.72 g, 44 mmol) and mechlorethamine hydrochloride (4.32 g, 22 mmol). Under nitrogen, the reaction was heated to reflux and stirred for another 2 hr. The reaction mixture was then allowed to cool to room temperature and was stirred overnight. A thin layer chromatography (tlc) using methylene chloride: methanol: conc. ammonium hydroxide (90:10:1) showed the more polar product (Rf 0.25) with only a trace of the starting naphthol. Silica gel (4.5 g) was added and the reaction mixture was concentrated in vacuo to a dry purple solid. This was added to a column of silica gel (ca. 400 g) and eluted with 2 L volumes of CH2Cl2, CH2Cl2 :CH3OH (40:1), CH2Cl2 :CH3OH:conc. NH4OH (20:1:0.1) and finally 4 L of CH2Cl2 :CH3OH:conc. NH4CH (10:1:0.1). The appropriate fractions were combined to yield a purple-black solid, 5.26 g, mp 184°-185° C.

후처리

  1. temperatureUnder nitrogen, the reaction was heated
  2. temperatureto reflux
  3. stirringwas stirred overnight
  4. additionSilica gel (4.5 g) was added
  5. concentrationthe reaction mixture was concentrated in vacuo to a dry purple solid
  6. additionThis was added to a column of silica gel (ca. 400 g)
  7. washeluted with 2 L volumes of CH2Cl2, CH2Cl2 :CH3OH (40:1), CH2Cl2
  8. customto yield a purple-black solid, 5.26 g, mp 184°-185° C.

출처 및 근거

ORD 기록
ord-347a497a622b47bc996cee0da2273737
출처 데이터셋
uspto-grants-1998_10
특허 번호
US05821245

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