Sodium Hydroxide → 5,6-Dihydro-8-methoxy-2-[(6-phenylpyridin-2-yl)-methylthio]-4H-imidazo[4,5,1-ij]quinoline

HRID 256306Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 256306
Cl.Cl[CH2:3][C:4]1[CH:9]=[CH:8][CH:7]=[C:6]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[N:5]=1.[CH3:16][O:17][C:18]1[CH:19]=[C:20]2[C:25]3=[C:26]([NH:28][C:29](=[S:30])[N:24]3[CH2:23][CH2:22][CH2:21]2)[CH:27]=1.[OH-].[Na+]>C(O)C>[CH3:16][O:17][C:18]1[CH:19]=[C:20]2[C:25]3=[C:26]([N:28]=[C:29]([S:30][CH2:3][C:4]4[CH:9]=[CH:8][CH:7]=[C:6]([C:10]5[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=5)[N:5]=4)[N:24]3[CH2:23][CH2:22][CH2:21]2)[CH:27]=1

Komponenten

5

Versuchsvorschrift

2-Chloromethyl-6-phenylpyridine hydrochloride 1.942 g, 8.1 mmol) was added to a solution of 5,6-dihydro-8-methoxy-4H-imidazo[4,5,1-ij]quinoline-2[1H]-thione (1.78 g, 8.1 mmol) in ethanol (16 ml) and 1N-sodium hydroxide (16.2 ml). The mixture was heated under reflux for 15 seconds and cooled to room temperature. The ethanol was removed by evaporation in vacuo and the aqueous mixture extracted with dichloromethane (2×150 ml). The extracts were dried (MgSO4) and evaporated in vacuo to give a brown solid which was recrystallised from MeOH to give the title compound as the quarter hydrate (2.77 g, 88%), mp 134°-135° C. (Found: C, 70.5; H, 5.8; N, 10.4; C23H21N3OS1/4H2O requires C, 70.5; H, 5.5; N, 10.7%).

Aufarbeitung

  1. temperatureThe mixture was heated
  2. temperatureunder reflux for 15 seconds
  3. customThe ethanol was removed by evaporation in vacuo
  4. extractionthe aqueous mixture extracted with dichloromethane (2×150 ml)
  5. dry with materialThe extracts were dried (MgSO4)
  6. customevaporated in vacuo
  7. customto give a brown solid which
  8. customwas recrystallised from MeOH

Quellen und Nachweise

ORD-Eintrag
ord-31386b8b23594ff7ae6794e70eea2862
Quelldatensatz
uspto-grants-1987_10
Patentnummer
US04703044

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