Acetic Acid → 8,9-dihydro-7-[(5-methyl-1H-imidazol-4-yl)methylene]pyrido[1,2-a]indol-6(7H)-one

HRID 1681751Notes

Reaction equation

[CH3:1][C:2]1[N:6](C(C2C=CC=CC=2)(C2C=CC=CC=2)C2C=CC=CC=2)[CH:5]=[N:4][C:3]=1[CH:26]=[C:27]1[C:39](=[O:40])[N:31]2[C:32]3[C:37]([CH:38]=[C:30]2[CH2:29][CH2:28]1)=[CH:36][CH:35]=[CH:34][CH:33]=3.C(O)(=O)C>O>[CH3:1][C:2]1[NH:6][CH:5]=[N:4][C:3]=1[CH:26]=[C:27]1[C:39](=[O:40])[N:31]2[C:32]3[C:37]([CH:38]=[C:30]2[CH2:29][CH2:28]1)=[CH:36][CH:35]=[CH:34][CH:33]=3

Participants

Conditions

Temperature: 80 °C

Procedure

A mixture of 8,9-dihydro-7-[(5-methyl-1-trityl-1H-imidazol-4-yl)methylene]pyrido[1,2-a]indol-6(7H)-one (21.28 g), acetic acid (500 ml), and water (80 ml) was stirred at 80° C. for 1 hour and 10 minutes. After evaporation of the solvent, the residue was diluted with water, neutralized with aqueous sodium bicarbonate solution and 3N aqueous sodium hydroxide solution, and extracted with chloroform to give precipitates. The precipitates were collected, washed with water and chloroform, and dried to give 8,9-dihydro-7-[(5-methyl-1H-imidazol-4-yl)methylene]pyrido[1,2-a]indol-6(7H)-one (5.8 g). The chloroform layer separated was washed with water and brine, dried over anhydrous magnesium sulfate, and evaporated to 50 ml. The chloroform solution was diluted with toluene and allowed to stand at room temperature overnight. The crystals were collected and washed with toluene to give a second crop of 8,9-dihydro-7-[(5-methyl-1H-imidazol-4-yl)methylene]pyrido[1,2-a]indol-6 (7H)-one (5.2 g).

Workup

customAfter evaporation of the solvent
additionthe residue was diluted with water
extractionextracted with chloroform
customto give
customprecipitates
customThe precipitates were collected
washwashed with water and chloroform
customdried

Sources & evidence

ORD record: ord-615f67d725a343f3b7fa07bcc19d39f5
Source dataset: uspto-grants-1992_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US05173493

Reaction notes

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