2-Pyridinecarboxaldehyde → HCID 59054371, compound

Reaction equation

[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[O:12][CH2:13][C:14]([CH3:17])([NH2:16])[CH3:15].[N:18]1[CH:23]=[CH:22][CH:21]=[CH:20][C:19]=1[CH:24]=O>>[Cl:1][C:2]1[C:11]2[C:6](=[CH:7][CH:8]=[CH:9][CH:10]=2)[CH:5]=[CH:4][C:3]=1[O:12][CH2:13][C:14]([CH3:17])([NH:16][CH2:24][C:19]1[CH:20]=[CH:21][CH:22]=[CH:23][N:18]=1)[CH3:15]

Participants

Reactant 2

HCID 142732-Pyridinecarboxaldehyde

HCID 681517292-(1-Chloronaphthalen-2-yloxy)-1,1-dimethylethylamine

Product 1

HCID 59054371HCID 59054371, compoundYield 34%

Procedure

Prepared from 1-[(1-chloronaphthalen-2-yl)oxy]-2-methylpropan-2-amine and pyridine-2 carbaldehyde in 34% yield as a colourless oil.

Sources & evidence

ORD record: ord-5e2a4e35e6014c5da6e1cb986c02fe30
Source dataset: uspto-grants-2014_12
DOI: 10.6084/m9.figshare.5104873.v1
Patent number: US08906946B2

Reaction notes

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