Diazosulfide compound and application in plant cell thereof
A technology of benzothiadiazoles and plant cells, which is applied in the fields of plant cells and organic chemistry, can solve the problems of resource scarcity and slow growth of yew, and achieve the effect of promoting growth
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Embodiment 1
[0013] Synthesis of 7-carboxybenzo-1,2,3-thiadiazole trifluoroethyl ester (compound 1):
[0014] Mix 7-carboxybenzothiadiazole (3.3mmol) and 8ml thionyl chloride, add a drying tube and a tail gas absorption device, heat the oil bath to 80-100°C, and keep it for 7-8 hours. After cooling to room temperature, the unreacted thionyl chloride was distilled off under reduced pressure to obtain a somewhat sticky solid, which was dissolved in toluene for further use. Measure 4ml of trifluoroethanol and 4ml of dry toluene and mix them in a small flask, add triethylamine, slowly add acid chloride toluene solution dropwise under stirring. Stir at room temperature for 2-4 hours. The reaction mixture was poured into ice water, extracted with ethyl acetate and washed with NaHCO 3 Wash once with saturated solution, twice with water, anhydrous MgSO 4 dry. Filter and concentrate to obtain a yellow-brown solid, which is separated by 300-400 mesh silica gel column chromatography. The obtaine...
Embodiment 2
[0018] Synthesis of benzo-1,2,3-thiadiazole-7-carboxylic acid-2,2,3,3,3-pentafluoropropyl ester (compound 2):
[0019] The acid chloride prepared by 7-carboxybenzothiadiazole (2.2mmol) (the preparation of the acid chloride is the same as in Example 1) was dissolved in toluene, and was added dropwise to a solution composed of pentafluoropropanol, toluene and triethylamine under stirring , the dropwise addition time is about 1 hour. The reaction was continued at room temperature for 5 hours. Pour the reaction mixture into water, extract with ethyl acetate, dilute K 2 CO 3 Solution washing, water washing, anhydrous MgSO 4 dry. Filtrate and concentrate to obtain a brown solution, which was separated by 300-400 mesh silica gel column chromatography to obtain 0.23 g of light yellow prismatic crystals, with a yield of 33.5% and a melting point of 79-80°C. 1 HNMR (SF: 500MHz, DMSO-d 6 )δ (ppm): 9.10-9.12 (d, 1H, J = 8.12Hz), 8.44-8.45 (d, 1H, J = 7.32Hz), 7.98-8.01 (t, 1H, J 1 ...
Embodiment 3
[0021] Synthesis of benzo-1,2,3-thiadiazole-7-carboxylic acid-pentafluorobenzyl ester (compound 3) The reaction conditions are the same as in Example 1 except pentafluorobenzyl alcohol. Obtained 0.42 g of pale yellow needle-like crystals with a yield of 53.0% and a melting point of 146-7°C. 1 HNMR (SF: 500MHz, DMSO-d 6 )δ (ppm): 9.03-9.05 (d, 1H, J = 8.10Hz), 8.39-8.41 (d, 1H, J = 7.35Hz), 7.91-7.94 (t, 1H, J 1 =7.65Hz,J 2 =7.83Hz), 5.62(s, 2H). HRMS, M + (m / e) 359.9983 (calc. 369.9992).
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