4-(2-Phenylethyl)piperidine → HCID 57647146, compound

HRID 1714881Notes

Reaction equation

HRID 1714881 reaction equation
Cl[C:2]1[N:7]=[N:6][C:5]([C:8]([NH:10][CH2:11][CH2:12][CH:13]([CH3:15])[CH3:14])=[O:9])=[CH:4][CH:3]=1.[C:16]1([CH2:22][CH2:23][CH:24]2[CH2:29][CH2:28][NH:27][CH2:26][CH2:25]2)[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=1>>[CH3:14][CH:13]([CH3:15])[CH2:12][CH2:11][NH:10][C:8]([C:5]1[N:6]=[N:7][C:2]([N:27]2[CH2:28][CH2:29][CH:24]([CH2:23][CH2:22][C:16]3[CH:21]=[CH:20][CH:19]=[CH:18][CH:17]=3)[CH2:25][CH2:26]2)=[CH:3][CH:4]=1)=[O:9]

Participants

3

Reactant 2

HCID 43418954-(2-Phenylethyl)piperidineHCID 167337866-chloro-N-(3-methylbutyl)pyridazine-3-carboxamide

Product 1

HCID 57647146HCID 57647146, compound

Procedure

The title compound was prepared in the same manner as described for Example 16 from 6-chloro-N-(3-methylbutyl)pyridazine-3-carboxamide and 4-(2-phenylethyl)piperidine. MS (+ESI) m/z 381 (MH+).

Sources & evidence

ORD record
ord-fc8efaff230d45e9827487a110b4b1c7
Source dataset
uspto-grants-2010_09
Patent number
US07799787B2

Reaction notes

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