223796-90-5 → HCID 11507869, compound

HRID 1180502Notes

Reaction equation

HRID 1180502 reaction equation
[Cl:1][C:2]1[CH:3]=[C:4]([N:8]2[CH2:14][CH2:13][CH2:12][NH:11][CH2:10][CH2:9]2)[CH:5]=[N:6][CH:7]=1.BrC1C=C(N2CCCN([C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30])CC2)C=NC=1>>[Cl:1][C:2]1[CH:3]=[C:4]([N:8]2[CH2:14][CH2:13][CH2:12][N:11]([C:29]([O:31][C:32]([CH3:35])([CH3:34])[CH3:33])=[O:30])[CH2:10][CH2:9]2)[CH:5]=[N:6][CH:7]=1

Participants

3

Reactant 2

HCID 11701287223796-90-5HCID 11717372HCID 11717372, compound

Product 1

HCID 11507869HCID 11507869, compound

Procedure

Was prepared from 1-(5-Chloro-3-pyridyl)-homopiperazine according to 1-(5-Bromo-3-pyridyl)-4-tert-butoxycarbonylhomopiperazine.

Sources & evidence

ORD record
ord-ce28ffa10ecf4658ad57adaf1c27039b
Source dataset
uspto-grants-2007_10
Patent number
US07282494B2

Reaction notes

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