Preparation method of thiazole derivative
A technology for thiazoles and products, which is applied in the field of new preparation of pharmaceutical intermediates, and can solve problems such as difficult synthesis
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[0023] (1) Synthesis of 6-chloro-2,3-dihydrobenzo[b][1,4]dioxine
[0024] Add 30g of 4-chlorocatechol to 400ml of N,N-dimethylformamide, add 21g of anhydrous potassium carbonate, then add 35g of 1,2-dibromoethane, heat under reflux and stir for 15 hours, then cool to room temperature , concentrated to remove most of N,N-dimethylformamide, added water and ethyl acetate, extracted, separated, dried, concentrated, and the residue was separated on a column to obtain 38g of 6-chloro-2,3-dihydrobenzo [b][1,4]dioxine.
[0025] (2) Synthesis of 2-bromo-1-(7-chloro-2,3-dihydrobenzo[b][1,4]dioxin-6-yl)ethane
[0026] Add 38g of 6-chloro-2,3-dihydrobenzo[b][1,4]dioxine into 500ml of dichloromethane, add 60g of bromoacetyl bromide, heat and reflux for 4 hours, and cool to At room temperature, add water again, extract and separate, collect the organic phase, separate, dry, concentrate, and separate the residue on a silica gel column to obtain 42g of 2-bromo-1-(7-chloro-2,3-dihydrobenzo[b...
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