1H-Imidazole-1-propanamine → 3(2-Chloro-5-thiophen-2-yl-pyrimidine-4-yl)-(3-imidazol-1-yl-propyl)-amine
Reaction equation
[Cl:1][C:2]1[N:7]=[C:6](Cl)[C:5](I)=[CH:4][N:3]=1.[N:10]1([CH2:15][CH2:16][CH2:17][NH2:18])[CH:14]=[CH:13][N:12]=[CH:11]1.CC1(C)C(C)(C)OB([C:27]2[S:28][CH:29]=[CH:30][CH:31]=2)O1>>[Cl:1][C:2]1[N:7]=[C:6]([CH:15]([N:10]2[CH:14]=[CH:13][N:12]=[CH:11]2)[CH2:16][CH2:17][NH2:18])[C:5]([C:27]2[S:28][CH:29]=[CH:30][CH:31]=2)=[CH:4][N:3]=1Participants
4
Procedure
Preparation according to procedures 2 and 3 with the use of 2,4-dichloro-5-iodo-pyrimidine, 3-imidazol-1-yl-propylamine and 4,4,5,5-tetramethyl-2-(2-thienyl)-1,3,2-dioxaborolane.
Workup
- customPreparation
Sources & evidence
- ORD record
- ord-22736563edbc4b00aee5897ed2a605ea
- Source dataset
- uspto-grants-2010_11
- Patent number
- US07825128B2
Reaction notes
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