1,2-Dimethoxyethane → 2-[2-(4-Chloro-phenyl)-5-ethyl-thiazol-4-yl]-cyclopentane-1,3-dione
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[S:9][C:10]([CH:13](OC3CCC(=O)C=3)[CH3:14])=[CH:11][N:12]=2)=[CH:4][CH:3]=1.[N-](S(C(F)(F)F)(=O)=O)S(C(F)(F)F)(=O)=[O:24].[CH2:37]([N+]1C=CN(C)C=1)[CH2:38][CH2:39][CH3:40].[CH3:47][O:48]CCOC>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([C:8]2[S:9][C:10]([CH2:13][CH3:14])=[C:11]([CH:37]3[C:38](=[O:24])[CH2:39][CH2:40][C:47]3=[O:48])[N:12]=2)=[CH:6][CH:7]=1Participants
4
Conditions
- Temperature
- 230 °C
Procedure
To a solution of 3-{1-[2-(4-Chloro-phenyl)-thiazol-5-yl]-ethoxy}-cyclopent-2-enone (2.29 g, 7.16 mmol) in ethylene glycol dimethyl ether (10 ml) was added 1-butyl-3-methylimidazolium bis(trifluoromethylsulphonyl)imide (100 μl) and the reaction heated to 230° C. by microwave irradiation for 30 minutes. The crude reaction mixture was dry loaded onto silica and purified by flash chromatography to give 2-[2-(4-Chloro-phenyl)-5-ethyl-thiazol-4-yl]-cyclopentane-1,3-dione (681 mg).
Workup
- customThe crude reaction mixture
- customwas dry
- custompurified by flash chromatography
Sources & evidence
- ORD record
- ord-74a96bd44cb644aaa41592698f7d5aeb
- Source dataset
- uspto-grants-2015_06
- Patent number
- US09051300B2
Reaction notes
Loading…