(S)-1-Cyclopropyl-7-[3-[[(1,1-dimethylethoxy)carbonyl]amino]-1-pyrrolidinyl]-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, ethyl ester → (S)-7-[3-(Amino)-1-pyrrolidinyl]-1-cyclopropyl-6,8-difluoro-1,4-dihydro-4-oxo-3-quinolinecarboxylic acid, ethyl ester

HRID 232048Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 232048
[CH:1]1([N:4]2[C:13]3[C:8](=[CH:9][C:10]([F:28])=[C:11]([N:15]4[CH2:19][CH2:18][C@H:17]([NH:20]C(OC(C)(C)C)=O)[CH2:16]4)[C:12]=3[F:14])[C:7](=[O:29])[C:6]([C:30]([O:32][CH2:33][CH3:34])=[O:31])=[CH:5]2)[CH2:3][CH2:2]1>FC(F)(F)C(O)=O>[NH2:20][C@H:17]1[CH2:18][CH2:19][N:15]([C:11]2[C:12]([F:14])=[C:13]3[C:8]([C:7](=[O:29])[C:6]([C:30]([O:32][CH2:33][CH3:34])=[O:31])=[CH:5][N:4]3[CH:1]3[CH2:2][CH2:3]3)=[CH:9][C:10]=2[F:28])[CH2:16]1

Komponenten

3

Versuchsvorschrift

A solution of 23.9 g (50 mmol) of (S)-1-cyclopropyl-7-[3-[[(1,1-dimethylethoxy)carbonyl]amino]-1-pyrrolidinyl]-6,8-difluoro-1,4-dihydro-4-oxo-3-quinoline carboxylic acid, ethyl ester in 150 ml of trifluoroacetic acid was stirred at room temperature for four hours. The solvent was removed in vacuo and the residue was triturated with 5% sodium bicarbonate. The solid was removed by filtration, washed 5% sodium bicarbonate, water and dried in vacuo to give 17.8 g of the title compound, mp 227°-228°.

Aufarbeitung

  1. customThe solvent was removed in vacuo
  2. customthe residue was triturated with 5% sodium bicarbonate
  3. customThe solid was removed by filtration
  4. washwashed 5% sodium bicarbonate, water
  5. customdried in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-6c71886f83b546709b8e37067f8b0f7f
Quelldatensatz
uspto-grants-1989_07
Patentnummer
US04851418

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