Ethyl 4-oxo-1-piperidinecarboxylate → HCID 67568850, compound
Reaction equation
[ClH:1].Cl.[NH2:3][C:4]1[CH:12]=[C:11]([F:13])[CH:10]=[C:9]([F:14])[C:5]=1[C:6]([NH2:8])=[NH:7].O=[C:16]1[CH2:21][CH2:20][N:19]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH2:18][CH2:17]1>>[ClH:1].[NH2:7][C:6]1[C:5]2[C:4](=[CH:12][C:11]([F:13])=[CH:10][C:9]=2[F:14])[NH:3][C:16]2([CH2:21][CH2:20][N:19]([C:22]([O:24][CH2:25][CH3:26])=[O:23])[CH2:18][CH2:17]2)[N:8]=1Participants
3
Procedure
This was prepared by the method of Example 173 using 2-anino-4,6-difluorobenzamidine dihydrochloride (Example H) and ethyl 4-oxopiperidine-1-carboxylate to give the title compound, m.p. 245°-246° C.
Sources & evidence
- ORD record
- ord-f2ad2149346c4a4b902b73af10aab04a
- Source dataset
- uspto-grants-1999_03
- Patent number
- US05883102
Reaction notes
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