Benzyl Bromide → HCID 20359956, compound
Reaction equation
[OH:1][N:2]1[C:10]2[C:5](=[N:6][CH:7]=[C:8]([Cl:11])[CH:9]=2)[N:4]=[C:3]1[C:12]([F:15])([F:14])[F:13].[CH2:16](Br)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.C(=O)([O-])[O-].[K+].[K+]>C(O)C>[CH2:16]([O:1][N:2]1[C:10]2[C:5](=[N:6][CH:7]=[C:8]([Cl:11])[CH:9]=2)[N:4]=[C:3]1[C:12]([F:15])([F:14])[F:13])[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
1-Hydroxy-6-chloro-2-(trifluoromethyl)-1H-imidazo-(4,5-b) pyridine (5 grams), 10 milliliters of benzyl bromide, 20 grams of anhydrous potassium carbonate, andd 100 milliliters of ethanol were mixed, heated to reflux, and refluxed for 1 hour. The reaction mixture was then filtered, evaporated under vacuum, and extracted with diethyl ether. The extract was filtered and evaporated under vacuum yielding a dark oil which on standing crystallized as the desired 1-benzyloxy-6-chloro-2-(trifluoromethyl)-1H-imadazo (4,5-b) pyridine. It was recrystallized from a mixture of acetone and petroleum ether boiling at 60°-80° C., m.p., 107°-09° C.
Workup
- temperatureheated
- temperatureto reflux
- temperaturerefluxed for 1 hour
- filtrationThe reaction mixture was then filtered
- customevaporated under vacuum
- extractionextracted with diethyl ether
- filtrationThe extract was filtered
- customevaporated under vacuum
- customyielding a dark oil which
- customon standing crystallized as the desired 1-benzyloxy-6-chloro-2-(trifluoromethyl)-1H-imadazo (4,5-b) pyridine
- customIt was recrystallized from a mixture of acetone and petroleum ether boiling at 60°-80° C., m.p., 107°-09° C
Sources & evidence
- ORD record
- ord-88e1b7c4da51499eadc8b374563a6c59
- Source dataset
- uspto-grants-1977_10
- Patent number
- US04054573
Reaction notes
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