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, and 100 milliliters of ethanol were mixed, heated to reflux, and refluxed for one 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-imidazo(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 one 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-imidazo(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-02502fe986c24c99a467aa419afc0794
- Source dataset
- uspto-grants-1978_04
- Patent number
- US04082534
Reaction notes
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