6-Chloro-3-nitropyridin-2-ylamine → HCID 12086022, compound

HRID 396167Notes

Reaction equation

HRID 396167 reaction equation
[NH2:1][C:2]1[N:3]=[CH:4][C:5]([NH:16][CH2:17][CH2:18][NH2:19])=[N:6][C:7]=1[C:8]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][C:9]=1[Cl:15].Cl[C:21]1[N:26]=[C:25]([NH2:27])[C:24]([N+:28]([O-:30])=[O:29])=[CH:23][CH:22]=1>>[NH2:1][C:2]1[N:3]=[CH:4][C:5]([NH:16][CH2:17][CH2:18][NH:19][C:21]2[CH:22]=[CH:23][C:24]([N+:28]([O-:30])=[O:29])=[C:25]([NH2:27])[N:26]=2)=[N:6][C:7]=1[C:8]1[CH:13]=[CH:12][C:11]([Cl:14])=[CH:10][C:9]=1[Cl:15]

Participants

3

Reactant 2

HCID 27240356-Chloro-3-nitropyridin-2-ylamineHCID 12086021HCID 12086021, compound

Product 1

HCID 12086022HCID 12086022, compound

Procedure

The compound was prepared from [5-amino-6-(2,4-dichlorophenyl)pyrazin-2-yl](2-aminoethyl)amine and 6-chloro-3-nitro-2-pyridylamine in accordance to the procedure described for Example 6.

Sources & evidence

ORD record
ord-008bfae34e334472a1fa92634b12ffbc
Source dataset
uspto-grants-2003_08
Patent number
US06608063B2

Reaction notes

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