Sodium borohydride → HCID 54256453, compound
Reaction equation
[CH:1]1([N:4]2[C:13]3[C:8](=[CH:9][C:10]([F:15])=[C:11]([F:14])[CH:12]=3)[C:7](=[O:16])[CH:6]=[C:5]2C(O)=O)[CH2:3][CH2:2]1.[BH4-].[Na+]>>[CH:1]1([N:4]2[C:13]3[C:8](=[CH:9][C:10]([F:15])=[C:11]([F:14])[CH:12]=3)[C:7](=[O:16])[CH2:6][CH2:5]2)[CH2:3][CH2:2]1Participants
3
Procedure
1-Cyclopropyl-6,7-difluoro-1,4-dihydro-4-oxoquinoline carboxylic acid(20 g) and sodium borohydride(11.5 g) were reacted in the same method as described in Preparation 1-A to give the yellow above-indicated compound(12 g).
Sources & evidence
- ORD record
- ord-ff8c4ed0fd9840b6ab3e83cf80202fef
- Source dataset
- uspto-grants-1997_09
- Patent number
- US05663331
Reaction notes
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