A kind of synthesis method of dye for blood cell analysis
A technology of blood cell analysis and synthesis method, which is applied in the field of synthesis of dyes for cell staining and blood cell analysis. It can solve the problems of low purity of target products, high raw material prices, and difficulty in removing them completely, and achieve excellent purity, rapid synthesis, and The effect of simple structure
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Embodiment 1
[0023] Embodiment one: the synthesis of the first intermediate product
[0024] Take 3 mmol of N,N’-dimethylformamidine into a test tube, then add 0.2 ml of acetic anhydride, stir and dissolve in an oil bath at 85°C (solution B). Then take 1mmol of 2,3-dimethylbenzothiazole methylsulfate into another test tube, add 1.5ml of acetic acid, stir and dissolve in an oil bath at 85°C (solution A).
[0025] In an oil bath at 85°C, add liquid A to liquid B drop by drop, stirring constantly. The mixed solution will gradually turn red during the dropwise addition, which means that A and B have started to react.
[0026] After the dropwise addition, the mixture was stirred and reacted in an oil bath at 85°C for 1.5 h. After the reaction, the mixture should be a dark red liquid.
[0027] After the mixture was cooled, the acetic acid and acetic anhydride in the mixture were removed by distillation under reduced pressure, and then about 20 ml of methanol was added to redissolve the mixture...
Embodiment 2
[0029] Embodiment two: the synthesis of the second intermediate product
[0030] Mix 5 mmol 1-octanol and 0.435 g pyridine with about 2 ml CH 2 Cl 2 (dichloromethane) mixed.
[0031] Mix 0.91 ml trifluoromethanesulfonic anhydride with 5 ml CH 2 Cl 2 Mix well, then store at -5°C~0°C and N 2 (Nitrogen) protection, dropwise added to 1-octanol, pyridine and CH 2 Cl 2 in the mixture. The dropwise addition process takes about 20 minutes. Too fast dropwise addition will cause the temperature to rise rapidly, which is not conducive to the progress of the reaction.
[0032] After the dropwise addition, the reaction was stirred at -10°C for 45 min. A pink product and a white solid (product of the reaction of trifluoromethanesulfonic anhydride and pyridine) appear during the reaction.
[0033] After the reaction, add an appropriate amount of CH 2 Cl 2 and water, which will dissolve the white solid, and the aqueous solution is removed after the layers are separated. The produc...
Embodiment 3
[0035] Embodiment three: the synthesis of the 3rd intermediate product
[0036] Take 3.34mmol intermediate product 2 and about 5 ml CH 2 Cl 2 (dichloromethane) mixed.
[0037] Add 3.34mmol 4-methylquinoline to the above mixture, N 2 Heated to reflux under protection for about 1 h.
[0038] Removal of CH by distillation under reduced pressure 2 Cl 2 , and then washed the product several times with anhydrous diethyl ether to remove impurities, and finally a light brown oil was obtained, which was the third intermediate product.
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