Acetaldehyde → (2,6-Dimethylimidazo[1,2-a]pyridin-3-yl)-(1,1,3,3-tetramethylbutyl)-amine

HRID 22802

Reaction equation

HRID 22802 reaction equation
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][N:3]=1.[CH3:9][C:10]([N+:17]#[C-:18])([CH3:16])[CH2:11][C:12]([CH3:15])([CH3:14])[CH3:13].[CH:19](=O)[CH3:20]>Cl(O)(=O)(=O)=O>[CH3:19][C:20]1[N:1]=[C:2]2[CH:7]=[CH:6][C:5]([CH3:8])=[CH:4][N:3]2[C:18]=1[NH:17][C:10]([CH3:16])([CH3:9])[CH2:11][C:12]([CH3:15])([CH3:14])[CH3:13]

Participants

5

Reactant 3

HCID 177AcetaldehydeHCID 153482-Amino-5-methylpyridineHCID 267251,1,3,3-Tetramethylbutyl isocyanide

Product 1

HCID 22591918(2,6-Dimethylimidazo[1,2-a]pyridin-3-yl)-(1,1,3,3-tetramethylbutyl)-amine

Reagents, catalysts & solvents 1

HCID 24247Perchloric AcidSolvent

Procedure

Compound (17) was prepared according to the general synthesis instructions from 1.0 ml of 2-amino-5-methylpyridine solution (0.1 M, DCM), 0.575 ml of 1,1,3,3-tetramethylbutyl isocyanide solution (0.2 M, DCM), 0.500 ml of acetaldehyde solution (0.3 M, DCM), and 10 μl of perchloric acid (w=20%).

Sources & evidence

ORD record
ord-1f6671239cb844e09ab80c3ea50d703f
Source dataset
uspto-grants-2005_02
Patent number
US06849642B2

Linked notes

Loading…