Potassium Carbonate → 9-Acetyl-8-hydroxy-1,2-dihydro-6-(3-dimethylaminopropyl)-cyclopenta[c]carbazole-3-one

HRID 1615047Notes

Reaction equation

HRID 1615047 reaction equation
[C:1]([C:4]1[C:16]([O:17]C)=[CH:15][C:14]2[N:13]([CH2:19][CH2:20][CH2:21][N:22]([CH3:24])[CH3:23])[C:12]3[CH:11]=[CH:10][C:9]4[C:25](=[O:28])[CH2:26][CH2:27][C:8]=4[C:7]=3[C:6]=2[CH:5]=1)(=[O:3])[CH3:2].Cl.N1C=CC=CC=1.C([O-])([O-])=O.[K+].[K+]>CN1C(=O)CCC1>[C:1]([C:4]1[C:16]([OH:17])=[CH:15][C:14]2[N:13]([CH2:19][CH2:20][CH2:21][N:22]([CH3:23])[CH3:24])[C:12]3[CH:11]=[CH:10][C:9]4[C:25](=[O:28])[CH2:26][CH2:27][C:8]=4[C:7]=3[C:6]=2[CH:5]=1)(=[O:3])[CH3:2]

Participants

5

Procedure

A solution of 9-acetyl-8-methoxy-1,2-dihydro-6-(3-dimethylaminopropyl)-cyclopenta[c]carbazole-3-one (84) (22 g, 58.2 mmol, 1 eq) and pyridine hydrochloride (134.4 g, 1164 mmol, 20 eq) in NMP (150 mL) was refluxed for 10 h. The reaction mixture was cooled to room temperature and poured into the 10% aqueous K2CO3 solution (3 L). The precipitated dark green solid was filtered off, washed with water (5×100 mL) and dried. The crude product was purified by column chromatography (eluent 10%-20% MeOH in EtOAc) to give 7.81 (37%) of pure 9-acetyl-8-hydroxy-1,2-dihydro-6-(3-dimethylaminopropyl)-cyclopenta[c]carbazole-3-one as a pale yellow solid.

Workup

  1. filtrationThe precipitated dark green solid was filtered off
  2. washwashed with water (5×100 mL)
  3. customdried
  4. customThe crude product was purified by column chromatography (eluent 10%-20% MeOH in EtOAc)

Sources & evidence

ORD record
ord-7d77b7b41e544fe4956b8dae26f65443
Source dataset
uspto-grants-2014_07
Patent number
US08765738B2

Reaction notes

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