2-Chloro-6-(1-piperazinyl)pyrazine → 2-[(3-Cyanobenzyl)Oxy]-6-(1-Piperazinyl)Pyrazine

HRID 1296667

Reaction equation

HRID 1296667 reaction equation
Cl[C:2]1[CH:7]=[N:6][CH:5]=[C:4]([N:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)[N:3]=1.[C:14]([C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][CH:23]=1)[CH2:19][OH:20])#[N:15]>>[C:14]([C:16]1[CH:17]=[C:18]([CH:21]=[CH:22][CH:23]=1)[CH2:19][O:20][C:2]1[CH:7]=[N:6][CH:5]=[C:4]([N:8]2[CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)[N:3]=1)#[N:15]

Participants

3

Reactant 2

HCID 1079922-Chloro-6-(1-piperazinyl)pyrazineHCID 27346773-(Hydroxymethyl)benzonitrile

Product 1

HCID 98573352-[(3-Cyanobenzyl)Oxy]-6-(1-Piperazinyl)Pyrazine

Procedure

Starting materials, 2-chloro-6-(1-piperazinyl)pyrazine and 3-cyanobenzyl alcohol.

Sources & evidence

ORD record
ord-f1a743b9cb9c42a78f506826b736b4a4
Source dataset
uspto-grants-2007_07
Patent number
US07247633B2

Linked notes

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