4-Aminophenethyl alcohol → 2-{4-[(5-Methyl-3-nitro-2-pyridinyl)amino]phenyl}ethanol

HRID 858408Notes

Reaction equation

HRID 858408 reaction equation
Cl[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][C:5]([CH3:11])=[CH:4][N:3]=1.[NH2:12][C:13]1[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][OH:21])=[CH:15][CH:14]=1>>[CH3:11][C:5]1[CH:6]=[C:7]([N+:8]([O-:10])=[O:9])[C:2]([NH:12][C:13]2[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][OH:21])=[CH:15][CH:14]=2)=[N:3][CH:4]=1

Participants

3

Reactant 2

HCID 669044-Aminophenethyl alcoholHCID 8183002-Chloro-5-methyl-3-nitropyridine

Product 1

HCID 218755422-{4-[(5-Methyl-3-nitro-2-pyridinyl)amino]phenyl}ethanol

Procedure

The title compound was prepared according to the procedure described in step 3 of Example 1 from 2-chloro-5-methyl-3-nitropyridine and 4-aminophenylethyl alcohol.

Sources & evidence

ORD record
ord-f2522155e2f2499bbc767c5a19119657
Source dataset
uspto-grants-2006_12
Patent number
US07148234B2

Reaction notes

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