N,N,N',N',N'',N''-Hexamethylmethanetriamine → HCID 178462501, compound
Reaction equation
[Br:1][C:2]1[CH:23]=[CH:22][C:5]2[N:6]([CH2:20][CH3:21])[C:7]([CH2:9][CH2:10][C:11]([C:13]3[CH:18]=[CH:17][CH:16]=[C:15]([F:19])[CH:14]=3)=O)=[N:8][C:4]=2[CH:3]=1.CN(C([N:31]([CH3:33])C)N(C)C)C.C(O)(=O)C.[NH2:38]N>CCO>[Br:1][C:2]1[CH:23]=[CH:22][C:5]2[N:6]([CH2:20][CH3:21])[C:7]([CH2:9][C:10]3[C:11]([C:13]4[CH:18]=[CH:17][CH:16]=[C:15]([F:19])[CH:14]=4)=[N:38][NH:31][CH:33]=3)=[N:8][C:4]=2[CH:3]=1Participants
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 60 °C
Procedure
A mixture of 3-(5-Bromo-1-ethyl-1H-benzoimidazol-2-yl)-1-(3-fluoro-phenyl)-propan-1-one (0.1 g, 0.27 mmol) and tris(dimethylamino)methane (0.077 g, 0.54 mmol) is heated at 60° C. in a sealed tube for 6 hours. The volatile material is removed in vacuo. EtOH (5 mL) and hydrazine acetate (1.1 mmol) are added to the residue. The mixture is heated at 120° C. for 2 hours. The solvent is removed. NaHCO3 (aq.) (10 mL) and DCM (30 mL) are added to the residue. The organic layer is separated and the aqueous layer is extracted with DCM (2×15 mL). The combined organic layers are dried and the solvent removed. The crude is purified by PTLC (ethyl acetate/Hexanes 1:1) to give 5-bromo-1-ethyl-2-[3-(3-fluoro-phenyl)-1H-pyrazol-4-ylmethyl]-1H-benzoimidazole as a solid. LRMS: calcd 399.3, found [M+1] 401.0.
Workup
- customThe volatile material is removed in vacuo
- temperatureThe mixture is heated at 120° C. for 2 hours
- customThe solvent is removed
- additionNaHCO3 (aq.) (10 mL) and DCM (30 mL) are added to the residue
- customThe organic layer is separated
- extractionthe aqueous layer is extracted with DCM (2×15 mL)
- customThe combined organic layers are dried
- customthe solvent removed
- customThe crude is purified by PTLC (ethyl acetate/Hexanes 1:1)
Sources & evidence
- ORD record
- ord-46aa61c393d84c23ba96c182990e6ccb
- Source dataset
- uspto-grants-2005_07
- Patent number
- US06916819B2
Reaction notes
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