4-Aminophenethyl alcohol → HCID 21875649, compound

HRID 858414Notes

Reaction equation

HRID 858414 reaction equation
Cl[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[C:6]([CH3:11])[C:5]([N+:12]([O-:14])=[O:13])=[CH:4][N:3]=1.[NH2:15][C:16]1[CH:21]=[CH:20][C:19]([CH2:22][CH2:23][OH:24])=[CH:18][CH:17]=1>>[CH3:11][C:6]1[C:5]([N+:12]([O-:14])=[O:13])=[CH:4][N:3]=[C:2]([NH:15][C:16]2[CH:21]=[CH:20][C:19]([CH2:22][CH2:23][OH:24])=[CH:18][CH:17]=2)[C:7]=1[N+:8]([O-:10])=[O:9]

Participants

3

Reactant 2

HCID 669044-Aminophenethyl alcoholHCID 21876360HCID 21876360, compound

Product 1

HCID 21875649HCID 21875649, compound

Procedure

The title compound was prepared according to the procedure described in step 3 of Example 1 from 2-chloro-4-methyl-3,5-dinitropyridine. (Czuba, Rocz. Chem., 1967, 41, 479) and 4-aminophenylethyl alcohol.

Sources & evidence

ORD record
ord-019206bb3a8444cb8e7e315d43ec13ed
Source dataset
uspto-grants-2006_12
Patent number
US07148234B2

Reaction notes

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