4-(4-Fluoro-benzyl)-piperidine → HCID 69100364, compound

HRID 2115081Notes

Reaction equation

HRID 2115081 reaction equation
Cl[CH2:2][C:3]([NH:5][C:6]1[CH:14]=[C:13]2[C:9]([CH:10]=[N:11][NH:12]2)=[CH:8][CH:7]=1)=[O:4].[F:15][C:16]1[CH:28]=[CH:27][C:19]([CH2:20][CH:21]2[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]2)=[CH:18][CH:17]=1>C(OCC)C>[F:15][C:16]1[CH:17]=[CH:18][C:19]([CH2:20][CH:21]2[CH2:22][CH2:23][N:24]([CH2:2][C:3]([NH:5][C:6]3[CH:14]=[C:13]4[C:9]([CH:10]=[N:11][NH:12]4)=[CH:8][CH:7]=3)=[O:4])[CH2:25][CH2:26]2)=[CH:27][CH:28]=1

Participants

4

Reactant 2

HCID 36998414-(4-Fluoro-benzyl)-piperidineHCID 5053143HCID 5053143, compound

Product 1

HCID 69100364HCID 69100364, compound

Reagents, catalysts & solvents 1

HCID 3283Diethyl EtherSolvent

Procedure

The title compound is prepared from 2-chloro-N-(1H-indazol-6-yl)-acetamide and 4-(4-fluoro-benzyl)-piperidine according to the method described in Example 142b. Melting Point: 135-137° C. (diethylether)

Sources & evidence

ORD record
ord-5fb93a79921c40aba4fea3c0d9644952
Source dataset
uspto-grants-2008_10
Patent number
US07435744B2

Reaction notes

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