Sodium hydride → HCID 15021590, compound
Reaction equation
[CH:1]1([N:4]2[C:13]3[C:8](=[C:9]([NH2:16])[CH:10]=[C:11](F)[C:12]=3[F:14])[C:7](=[O:17])[C:6]([C:18]([OH:20])=[O:19])=[CH:5]2)[CH2:3][CH2:2]1.[NH:21]1[CH2:26][CH2:25][CH:24]([OH:27])[CH2:23][CH2:22]1.[H-].[Na+]>>[NH:21]1[CH2:26][CH2:25][CH:24]([O:27][C:11]2[C:12]([F:14])=[C:13]3[C:8]([C:7](=[O:17])[C:6]([C:18]([OH:20])=[O:19])=[CH:5][N:4]3[CH:1]3[CH2:3][CH2:2]3)=[C:9]([NH2:16])[CH:10]=2)[CH2:23][CH2:22]1Participants
4
Procedure
1-Cyclopropyl-5-amino-7,8-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylic acid, 4-piperidinol and sodium hydride were reacted and treated in a similar manner to Example 9, whereby the title compound was obtained as colorless powder.
Sources & evidence
- ORD record
- ord-9ccc395e383d4504bf33da80afcc6fe1
- Source dataset
- uspto-grants-1992_10
- Patent number
- US05153203
Reaction notes
Loading…