HCID 69099830, compound → HCID 69100333, compound

HRID 2114975Notes

Reaction equation

HRID 2114975 reaction equation
[F:1][C:2]1[CH:28]=[CH:27][C:5]([CH2:6][CH:7]2[CH2:12][CH2:11][N:10]([C:13](=[O:26])[C:14]([NH:16][C:17]3[CH:22]=[CH:21][CH:20]=[C:19]([N+:23]([O-])=O)[CH:18]=3)=[O:15])[CH2:9][CH2:8]2)=[CH:4][CH:3]=1>C(OCC)C>[NH2:23][C:19]1[CH:18]=[C:17]([NH:16][C:14](=[O:15])[C:13]([N:10]2[CH2:11][CH2:12][CH:7]([CH2:6][C:5]3[CH:27]=[CH:28][C:2]([F:1])=[CH:3][CH:4]=3)[CH2:8][CH2:9]2)=[O:26])[CH:22]=[CH:21][CH:20]=1

Participants

3

Procedure

The title compound is prepared from 2-[4-(4-fluoro-benzyl)-piperidin-1-yl]-N-(3-nitro-phenyl)-2-oxo-acetamide (Example 15) according to the method described in Example 11. Melting Point: 117-120° C. (diethylether)

Sources & evidence

ORD record
ord-c862784676784f0c8836ac6d5bbd68a5
Source dataset
uspto-grants-2008_10
Patent number
US07435744B2

Reaction notes

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