4-Benzylpiperidine → HCID 69101095, compound

HRID 2115079Notes

Reaction equation

HRID 2115079 reaction equation
Cl[CH2:2][C:3]([NH:5][C:6]1[CH:7]=[C:8]2[C:12](=[CH:13][CH:14]=1)[NH:11][N:10]=[CH:9]2)=[O:4].[CH2:15]([CH:22]1[CH2:27][CH2:26][NH:25][CH2:24][CH2:23]1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>C(OCC)C>[CH2:15]([CH:22]1[CH2:27][CH2:26][N:25]([CH2:2][C:3]([NH:5][C:6]2[CH:7]=[C:8]3[C:12](=[CH:13][CH:14]=2)[NH:11][N:10]=[CH:9]3)=[O:4])[CH2:24][CH2:23]1)[C:16]1[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1

Participants

4

Procedure

The title compound is prepared from 2-chloro-N-(1H-indazol-5-yl)-acetamide and 4-benzyl-piperidine (Aldrich) according to the method described in Example 142b. Melting Point: 170-174° C. (diethylether)

Sources & evidence

ORD record
ord-562702db30c242d8ba323a79b178a105
Source dataset
uspto-grants-2008_10
Patent number
US07435744B2

Reaction notes

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