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

HRID 497041Notes

Reaction equation

HRID 497041 reaction equation
[NH2:1][CH2:2][CH2:3][NH:4][C:5]1[N:6]=[C:7]([C:12]2[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=2[Cl:19])[C:8]([NH2:11])=[N:9][CH:10]=1.Cl[C:21]1[N:26]=[C:25]([NH2:27])[C:24]([N+:28]([O-:30])=[O:29])=[CH:23][CH:22]=1>>[NH2:27][C:25]1[N:26]=[C:21]([NH:1][CH2:2][CH2:3][NH:4][C:5]2[N:6]=[C:7]([C:12]3[CH:17]=[CH:16][C:15]([Cl:18])=[CH:14][C:13]=3[Cl:19])[C:8]([NH2:11])=[N:9][CH:10]=2)[CH:22]=[CH:23][C:24]=1[N+:28]([O-:30])=[O:29]

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 N5-(2-aminoethyl)-3-(2,4-dichlorophenyl)pyrazine-2,5-diamine and 6-chloro-3-nitro-2-pyridylamine in accordance to the procedure described for Example 6.

Sources & evidence

ORD record
ord-c793808a5d6a4a378e6359c6e159d5fa
Source dataset
uspto-grants-2005_09
Patent number
US06949547B2

Reaction notes

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