2-Chloro-5-nitropyridine → 4-[3-Imidazolyl-6-({2-[(5-nitro(2-pyridyl))amino]ethyl}amino)-2-pyridyl]benzene-carbonitrile

HRID 31915

반응식

HRID 31915 반응식
[C:1]([C:3]1[CH:12]=[CH:11][C:6]([C:7](=O)[CH2:8]Br)=[CH:5][CH:4]=1)#[N:2].[O:13]=[N+:14]([O-:16])[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[O-][N+](=O)[O-].[Ce+4].[NH4+].[NH4+].Cl[C:41]1C=C[C:44]([N+:47]([O-])=O)=[CH:43][N:42]=1.N[C:51]1[N:56]=[C:55]([NH:57][CH2:58][CH2:59][NH:60][C:61]2[CH:66]=[CH:65]C(C3NC=CN=3)=C(C3C=CC(Cl)=CC=3Cl)[N:62]=2)[CH:54]=[CH:53][C:52]=1[N+]([O-])=O>O.C(O)(=O)C>[NH:42]1[CH:43]=[CH:44][N:47]=[C:41]1[C:8]1[C:7]([C:6]2[CH:11]=[CH:12][C:3]([C:1]#[N:2])=[CH:4][CH:5]=2)=[N:62][C:61]([NH:60][CH2:59][CH2:58][NH:57][C:55]2[CH:54]=[CH:53][C:52]([N+:14]([O-:16])=[O:13])=[CH:51][N:56]=2)=[CH:66][CH:65]=1

참가 물질

7

반응물 4

HCID 783082-Chloro-5-nitropyridineHCID 986544-(Bromoacetyl)benzonitrileHCID 180504Ceric ammonium nitrateHCID 22142808{2-[(6-Amino-5-nitro(2-pyridyl))amino]ethyl}[6-(2,4-dichlorophenyl)-5-imidazolyl(2-pyridyl)]amine

생성물 1

HCID 221429584-[3-Imidazolyl-6-({2-[(5-nitro(2-pyridyl))amino]ethyl}amino)-2-pyridyl]benzene-carbonitrile

시약·촉매·용매 2

HCID 176Acetic Acid용매HCID 962Water용매

실험 절차

4-[3-imidazolyl-6-({2-[(5-nitro(2-pyridyl))amino]ethyl}amino)-2-pyridyl]Benzenecarbonitrile was prepared from 4-cyanophenacyl bromide, CAN for the oxidation (1:1 acetic acid and water with heating at 80° C. for 1 hour), and 2-chloro-5-nitropyridine using the general method for {2-[(6-amino-5-nitro(2-pyridyl))amino]ethyl}[6-(2,4-dichlorophenyl)-5-imidazolyl(2-pyridyl)]amine.

출처 및 근거

ORD 기록
ord-1edb383ab3cc4fde8e34fdcb39c74736
출처 데이터셋
uspto-grants-2008_09
특허 번호
US07425557B2

연결된 노트

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