Dimethylamine → HCID 86586427, compound
Reaction equation
[N:1]1[CH:6]=[CH:5][C:4]([CH2:7]C#N)=[CH:3][CH:2]=1.C(OC([N:19]([CH3:21])[CH3:20])N(C)C)(C)(C)C.C[NH:23][CH3:24].[C:25](O)(C)(C)C>C(Cl)Cl.C(OCC)(=O)C>[CH3:21][N:19]([CH:7]=[C:4]1[CH:3]=[CH:2][N:1]=[C:6]([CH2:25][C:24]#[N:23])[CH2:5]1)[CH3:20]Participants
6
Procedure
7.52 g (63.7 mmol) of 4-pyridylacetonitrile and 11.09 g (63.7 mmol) of tert-butoxybis(dimethylamino)methane were stirred at 100° C. for 2 h. In the course of this, liberated dimethylamine and t-butanol were led off to the atmosphere by a slight reduced pressure flow by means of a vacuum pump. Flash chromatography (CH2Cl2/ethyl acetate 50:1→20:1) yielded the title compound.
Sources & evidence
- ORD record
- ord-870af5687530492e8d375befa3db4e26
- Source dataset
- uspto-grants-2004_02
- Patent number
- US06693102B2
Reaction notes
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