Water → 7-(4-Methylamino-1,3,3a,4,7,7a-hexahydro-isoindol-2-yl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-5-vinyl-3-quinolinecarboxylic acid

HRID 2258128Notes

Reaction equation

HRID 2258128 reaction equation
[CH:1]1([N:4]2[C:13]3[C:8](=[C:9]([CH:17]=[CH2:18])[C:10]([F:16])=[C:11](F)[C:12]=3[F:14])[C:7](=[O:19])[C:6]([C:20]([OH:22])=[O:21])=[CH:5]2)[CH2:3][CH2:2]1.[CH3:23][NH:24][CH:25]1[CH:33]=[CH:32][CH2:31][CH:30]2[CH:26]1[CH2:27][NH:28][CH2:29]2.C1N2CCN(CC2)C1.O>C(#N)C.CN(C)C=O>[CH3:23][NH:24][CH:25]1[CH:33]=[CH:32][CH2:31][CH:30]2[CH:26]1[CH2:27][N:28]([C:11]1[C:12]([F:14])=[C:13]3[C:8]([C:7](=[O:19])[C:6]([C:20]([OH:22])=[O:21])=[CH:5][N:4]3[CH:1]3[CH2:3][CH2:2]3)=[C:9]([CH:17]=[CH2:18])[C:10]=1[F:16])[CH2:29]2

Participants

7

Procedure

0.46 g of 1-cyclopropyl-6,7,8-trifluoro-1,4-dihydro-4-oxo-5-vinyl-3-quinolinecarboxylic acid, 0.34 g of 4-methylamino-1,3,3a,4,7,7a-hexahydro-isoindole and 0.18 g of DABCO are refluxed for 2 hours in a mixture of 3 ml of acetonitrile and 1.5 ml of dimethylformamide. At room temperature, the reaction mixture is treated with 20 ml of water, and the product is filtered off with suction, washed with water and dried. 0.5 g of 7-(4-methylamino-1,3,3a,4,7,7a-hexahydro-isoindol-2-yl)-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-5-vinyl-3-quinolinecarboxylic acid is obtained.

Workup

  1. filtrationthe product is filtered off with suction
  2. washwashed with water
  3. customdried

Sources & evidence

ORD record
ord-31231a65471946879dd4d709300554a5
Source dataset
uspto-grants-1997_08
Patent number
US05659038

Reaction notes

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