4-Aminophenethyl alcohol → HCID 21875729, compound

HRID 2077647Notes

Reaction equation

HRID 2077647 reaction equation
[Br:1][C:2]1[C:3]([CH3:13])=[N:4][C:5](Cl)=[C:6]([N+:9]([O-:11])=[O:10])[C:7]=1[CH3:8].[NH2:14][C:15]1[CH:20]=[CH:19][C:18]([CH2:21][CH2:22][OH:23])=[CH:17][CH:16]=1>>[Br:1][C:2]1[C:7]([CH3:8])=[C:6]([N+:9]([O-:11])=[O:10])[C:5]([NH:14][C:15]2[CH:20]=[CH:19][C:18]([CH2:21][CH2:22][OH:23])=[CH:17][CH:16]=2)=[N:4][C:3]=1[CH3:13]

Participants

3

Reactant 2

HCID 669044-Aminophenethyl alcoholHCID 21876108HCID 21876108, compound

Product 1

HCID 21875729HCID 21875729, compound

Procedure

The title compound was prepared according to the procedure described in step 3 of Example 1 from 3-bromo-6-chloro-2,4-dimethyl-5-nitropyridine (step 2) and 4-aminophenylethyl alcohol.

Sources & evidence

ORD record
ord-5ff9c96c8f2d4edd94d32d9dc26c8b3f
Source dataset
uspto-grants-2011_04
Patent number
US07928119B2

Reaction notes

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