4-Aminophenethyl alcohol → HCID 21876169, compound

HRID 858406Notes

Reaction equation

HRID 858406 reaction equation
Cl[C:2]1[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=[C:4]([O:11][CH3:12])[N:3]=1.[NH2:13][C:14]1[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][OH:22])=[CH:16][CH:15]=1>>[CH3:12][O:11][C:4]1[N:3]=[C:2]([NH:13][C:14]2[CH:19]=[CH:18][C:17]([CH2:20][CH2:21][OH:22])=[CH:16][CH:15]=2)[C:7]([N+:8]([O-:10])=[O:9])=[CH:6][CH:5]=1

Participants

3

Reactant 2

HCID 669044-Aminophenethyl alcoholHCID 27950292-Chloro-6-methoxy-3-nitropyridine

Product 1

HCID 21876169HCID 21876169, compound

Procedure

The title compound was prepared according to the procedure described in step 3 of Example 1 from 2-chloro-6-methoxy-3-nitropyridine and 4-aminophenylethyl alcohol.

Sources & evidence

ORD record
ord-8976597eeb4b4bc794f202036c363ec1
Source dataset
uspto-grants-2006_12
Patent number
US07148234B2

Reaction notes

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