2-Methoxyphenylhydrazine Hydrochloride → HCID 22048841, compound

HRID 1832612Notes

Reaction equation

HRID 1832612 reaction equation
O1CCO[CH:2]1[CH2:6][CH2:7][CH2:8][CH2:9][N:10]1[CH2:15][CH2:14][CH:13]([C:16]2[CH:17]=[C:18]([NH:22][C:23](=[O:27])[CH:24]([CH3:26])[CH3:25])[CH:19]=[CH:20][CH:21]=2)[CH2:12][CH2:11]1.Cl.[CH3:29][O:30][C:31]1[CH:36]=[CH:35][CH:34]=[CH:33][C:32]=1[NH:37]N>>[CH3:29][O:30][C:31]1[CH:36]=[CH:35][CH:34]=[C:33]2[C:32]=1[NH:37][CH:2]=[C:6]2[CH2:7][CH2:8][CH2:9][N:10]1[CH2:15][CH2:14][CH:13]([C:16]2[CH:17]=[C:18]([NH:22][C:23](=[O:27])[CH:24]([CH3:25])[CH3:26])[CH:19]=[CH:20][CH:21]=2)[CH2:12][CH2:11]1

Participants

3

Reactant 2

HCID 28494452-Methoxyphenylhydrazine HydrochlorideHCID 22048802N-(3-{1-[4-(1,3-dioxolan-2-yl)butyl]4-piperidinyl}phenyl)-2-methylpropanamide

Product 1

HCID 22048841HCID 22048841, compound

Procedure

Prepared by Procedure H and Scheme S using N-(3-{1-[4-(1,3-dioxolan-2-yl)butyl]-4-piperidinyl}phenyl)-2-methylpropanamide and 1-(2-methoxyphenyl)hydrazine hydrochloride: ESMS m/e: 434.0 (M+H)+.

Workup

  1. customPrepared by Procedure H and Scheme S

Sources & evidence

ORD record
ord-3dbc623b8ee74ca6bfc96f4a92826c53
Source dataset
uspto-grants-2006_06
Patent number
US07067534B1

Reaction notes

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