2-Chloro-3-nitrothiophene → [4-(2,4-Dichlorophenyl)-5-imidazolylpyrimidin-2-yl]{2-[(3-nitro (2-thienyl))amino]ethyl}amine

HRID 31844

Reaction equation

HRID 31844 reaction equation
ClC1C=C(Cl)C=CC=1C1C(N2C=CN=C2)=CN=C(CCN)N=1.Cl[C:24]1[S:25][CH:26]=[CH:27][C:28]=1[N+:29]([O-:31])=[O:30].[Cl:32][C:33]1[CH:38]=[C:37]([Cl:39])[CH:36]=[CH:35][C:34]=1[C:40]1[C:45]([C:46]2[NH:47][CH:48]=[CH:49][N:50]=2)=[CH:44][N:43]=[C:42]([NH:51][CH2:52][CH2:53][NH:54]C2C=CC([N+]([O-])=O)=C(OC)N=2)[N:41]=1>>[Cl:32][C:33]1[CH:38]=[C:37]([Cl:39])[CH:36]=[CH:35][C:34]=1[C:40]1[C:45]([C:46]2[NH:50][CH:49]=[CH:48][N:47]=2)=[CH:44][N:43]=[C:42]([NH:51][CH2:52][CH2:53][NH:54][C:24]2[S:25][CH:26]=[CH:27][C:28]=2[N+:29]([O-:31])=[O:30])[N:41]=1

Participants

4

Reactant 3

HCID 2201862-Chloro-3-nitrothiopheneHCID 22142635[4-(2,4-Dichlorophenyl)-5-imidazol-2-ylpyrimidin-2-yl]{2-[(6-methoxy-5-nitro(2-pyridyl)) amino]ethyl}amineHCID 571748954-(2,4-Dichlorophenyl)-5-imidazol-1-ylpyrimidin-2-ylethylamine

Product 1

HCID 57165746[4-(2,4-Dichlorophenyl)-5-imidazolylpyrimidin-2-yl]{2-[(3-nitro (2-thienyl))amino]ethyl}amine

Procedure

[4-(2,4-dichlorophenyl)-5-imidazolylpyrimidin-2-yl]{2-[(3-nitro(2-thienyl))amino]-ethyl}amine was prepared from [4-(2,4-dichlorophenyl)-5-imidazol-1-ylpyrimidin-2-ylethylamine and 2-chloro-3-nitrothiophene in accordance with the procedure described above for the preparation of [4-(2,4-dichlorophenyl)-5-imidazol-2-ylpyrimidin-2-yl]{2-[(6-methoxy-5-nitro(2-pyridyl))amino]ethyl}amine.

Sources & evidence

ORD record
ord-9346bf19280a4b0991d583485fd33fda
Source dataset
uspto-grants-2008_09
Patent number
US07425557B2

Linked notes

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