反应 #4140847
相关文献 (1)
openreactiondata ↗doi:10.1039/C8SC04228D
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-640541e4f38a4cb9b51b453a7b45dbc5暂无可渲染的结构数据
CSC1=CC=CC=C1C(=O)Cl产品信息
邻甲硫基苯甲酸酰氯(CAS 1442-03-1)的产品身份、结构标识及相关反应资料,供化学中间体检索、研发和采购评估使用。
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12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-640541e4f38a4cb9b51b453a7b45dbc5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-2f71d978e3644808842db77037553a42反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-8ea8b7d7088d45a2b519a26df13f22ec反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: As described for Example 9, a mixture of 0.242 g of 2-(methylthio)benzoyl chloride (m.p. 61°-640° C.), 0.134 g of triethylamine and 0.314 g of 5-(4-aminobenzoyl)-6,11-dihydro-5H-dibenz[b,e]azepine in 10 ml of dichloromethane is stirred for 2.5 hours and worked up to give a solid. Trituration with ethyl acetate-hexane gives 0.150 g of crystals, m.p. 222°-225° C. to give a solid
来源 ID: ord-3628dd75c5cc46e080453cb888c20b79反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-640541e4f38a4cb9b51b453a7b45dbc5反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-640541e4f38a4cb9b51b453a7b45dbc5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: As described for Example 9, a mixture of 0.242 g of 2-(methylthio)benzoyl chloride (m.p. 61°-64° C.), 0.134 g of triethylamine and 0.314 g of 5-(4-aminobenzoyl)-6,11-dihydro-5H-dibenz[b,e]azepine in 10 ml of dichloromethane is stirred for 2.5 hours and worked up to give a solid. Trituration with ethyl acetate-hexane gives 0.150 g of crystals, m.p. 222°-225° C. to give a solid
来源 ID: ord-b2ddf5c21dff49c5b39b5713f70b85cb反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirred solution of 0.364 g of 2-(methylthio)benzoyl chloride 5 ml of methylene chloride is added 0.346 g of triethylamine at 0° C. After stirring for 3 minutes, 0,500 g of 10,11-dihydro-10-(4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine is added and stirring continued for 72 hours at room temperature. The reaction mixture is diluted with 45 ml of methylene chloride and washed with water, 2N citric acid, NaHCO 3, and brine. The reaction mixture is dried with N2SO4, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography using 1:1 ethyl acetate-hexane to give a solid which is crystallized from ethyl alcohol to give 0.480 g of the desired product as a white solid, m.p. 71°-174° C. stirring continued for 72 hours at room temperature washed with water, 2N citric acid, NaHCO 3, and brine The reaction mixture is dried with N2SO4 filtered evaporated in vacuo to give a solid which is purified by flash chromatography to give a solid which is crystallized from ethyl alcohol
来源 ID: ord-633e2354c8234581b8725ee487e6d84e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirred solution of 0.364 g of 2-(methylthio)benzoyl chloride 5 ml of methylene chloride is added 0.346 g of triethylamine at 0° C. After stirring for 3 minutes, 0,500 g of 10,11-dihydro-10-(4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine is added and stirring continued for 72 hours at room temperature. The reaction mixture is diluted with 45 ml of methylene chloride and washed with water, 2N citric acid, NaHCO 3, and brine. The reaction mixture is dried with N2SO4, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography using 1:1 ethyl acetate-hexane to give a solid which is crystallized from ethyl alcohol to give 0.480 g of the desired product as a white solid, m.p. 71°-174° C. stirring continued for 72 hours at room temperature washed with water, 2N citric acid, NaHCO 3, and brine The reaction mixture is dried with N2SO4 filtered evaporated in vacuo to give a solid which is purified by flash chromatography to give a solid which is crystallized from ethyl alcohol
来源 ID: ord-633e2354c8234581b8725ee487e6d84e反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: As described for Example 9, a mixture of 0.242 g of 2-(methylthio)benzoyl chloride (m.p. 61°-640° C.), 0.134 g of triethylamine and 0.314 g of 5-(4-aminobenzoyl)-6,11-dihydro-5H-dibenz[b,e]azepine in 10 ml of dichloromethane is stirred for 2.5 hours and worked up to give a solid. Trituration with ethyl acetate-hexane gives 0.150 g of crystals, m.p. 222°-225° C. to give a solid
来源 ID: ord-3628dd75c5cc46e080453cb888c20b79反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: As described for Example 9, a mixture of 0.242 g of 2-(methylthio)benzoyl chloride (m.p. 61°-640° C.), 0.134 g of triethylamine and 0.314 g of 5-(4-aminobenzoyl)-6,11-dihydro-5H-dibenz[b,e]azepine in 10 ml of dichloromethane is stirred for 2.5 hours and worked up to give a solid. Trituration with ethyl acetate-hexane gives 0.150 g of crystals, m.p. 222°-225° C. to give a solid
来源 ID: ord-3628dd75c5cc46e080453cb888c20b79反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a stirred solution of 0.364 g of 2-(methylthio)benzoyl chloride 5 ml of methylene chloride is added 0.346 g of triethylamine at 0° C. After stirring for 3 minutes, 500 g of 10,11-dihydro-10-(4-aminobenzoyl)-5H-pyrrolo[2,1-c][1,4]benzodiazepine is added and stirring continued for 72 hours at room temperature. The reaction mixture is diluted with 45 ml of methylene chloride and washed with water, 2N citric acid, NaCHO3, and brine. The reaction mixture is dried with Na2S04, filtered and evaporated in vacuo to give a solid which is purified by flash chromatography using 1:1 ethyl acetate-hexane to give a solid which is crystallized from ethyl alcohol to give 0.480 g of the desired product as a white solid, m.p. 171°-174° C. stirring continued for 72 hours at room temperature washed with water, 2N citric acid, NaCHO3, and brine The reaction mixture is dried with Na2S04 filtered evaporated in vacuo to give a solid which is purified by flash chromatography to give a solid which is crystallized from ethyl alcohol
来源 ID: ord-71798e73647a4439b94822b322491e45PubChem References
以下资料来自该化合物的公开数据库参考记录。
