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Acetone → 6-[2-(isopropylamino)ethyl]-10,11-dihydro-1H-dicyclopenta[c,g]carbazole-3,9(2H,6H)-dione

HRID 1615027
Notes
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Reaction equation

HRID 1615027 reaction equation
[NH2:1][CH2:2][CH2:3][N:4]1[C:16]2[CH:15]=[CH:14][C:13]3[C:17](=[O:20])[CH2:18][CH2:19][C:12]=3[C:11]=2[C:10]2[C:9]3[CH2:21][CH2:22][C:23](=[O:24])[C:8]=3[CH:7]=[CH:6][C:5]1=2.[CH3:25][C:26]([CH3:28])=O.C([O-])(O)=O.[Na+].Cl>C(Cl)Cl.CO.O1CCOCC1.C(Cl)(Cl)Cl.CO>[CH:26]([NH:1][CH2:2][CH2:3][N:4]1[C:16]2[CH:15]=[CH:14][C:13]3[C:17](=[O:20])[CH2:18][CH2:19][C:12]=3[C:11]=2[C:10]2[C:9]3[CH2:21][CH2:22][C:23](=[O:24])[C:8]=3[CH:7]=[CH:6][C:5]1=2)([CH3:28])[CH3:25]
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

9

Reactant 4

HCID 180AcetoneHCID 313Hydrochloric AcidHCID 516892Sodium BicarbonateHCID 453811166-(2-aminoethyl)-10,11-dihydro-1H-dicyclopenta[c,g]carbazole-3,9(2H,6H)-dione

Product 1

HCID 445191266-[2-(isopropylamino)ethyl]-10,11-dihydro-1H-dicyclopenta[c,g]carbazole-3,9(2H,6H)-dione

Reagents, catalysts & solvents 4

HCID 887
Methanol
Solvent
2×
HCID 6344DichloromethaneSolvent3×
HCID 312751,4-DioxaneSolvent
HCID 21584188Chloroform methanolSolvent

Procedure

Crude compound 59 (1.69 g) was suspended in CH2Cl2 (200 mL). Then acetone (4 mL) and STAB (3.4 g) were added. The mixture was stirred for 24 h (TLC monitoring, eluent: CHCl3-MeOH, 9:1), then poured into an aqueous NaHCO3 solution. Then, another portion of CH2Cl2 and MeOH was added. The organic layer was separated, evaporated, washed with MeCN and ether. Yield of Example 8: 0.759 g. For the preparation of hydrochloride, the isolated product was suspended in a mixture of CH2Cl2 and MeOH, then a solution of HCl in dioxane was added. The resulting mixture was evaporated to dryness, and ethanol was added to the residue. The ethanolic solution was refluxed and cooled, and the precipitate was filtered. Yield of compound Example 8 hydrochloride: 0.684 g. 1H-NMR (DMSO-D6) spectrum: δ 1.24 (6H, d, J=6.6 Hz); 2.77-2.79 (4H, m); 3.34-3.43 (3H, m); 3.81-3.84 (4H, m); 4.91 (2H, t, J=7.3 Hz); 7.83 (2H, d, J=8.6 Hz); 7.91 (2H, d, J=8.6 Hz); 9.11 (2H, br. s). ELSD: 100%, ESI-MS: m/z 360 [M+H].+

Workup

  1. customThe organic layer was separated
  2. customevaporated
  3. washwashed with MeCN and ether
  4. customFor the preparation of hydrochloride
  5. customThe resulting mixture was evaporated to dryness, and ethanol
  6. additionwas added to the residue
  7. temperatureThe ethanolic solution was refluxed
  8. temperaturecooled
  9. filtrationthe precipitate was filtered

Sources & evidence

ORD record
ord-5bf5a18a85a948cdb93ff2eb37b576e7
Source dataset
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08765738B2

Reaction notes

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On this pageParticipantsProcedureWorkupSources & evidenceReaction notes