反应 #4057715
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-f7394d1444f1468ca14c30a10f12d7e7暂无可渲染的结构数据
C1=CC(=C(C=C1C(=O)N)I)Cl产品信息
4-氯-3-碘苯甲酰胺(CAS 791137-24-1)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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5 条反应 · 5 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f7394d1444f1468ca14c30a10f12d7e7反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-f7394d1444f1468ca14c30a10f12d7e7反应条件: temp:80.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To 6-Bromo-1-morpholinophthalazine (0.20 g, 680 μmol), 1,1′-bis(diphenylphosphino)ferrocene-palladium dichloride (50 mg, 68 μmol), potassium acetate (200 mg, 2040 μmol), and 4,4,5,5-tetramethyl-2-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1,3,2-dioxaborolane (207 mg, 816 μmol) was added 1,4-dioxane (6.80 mL) and the mixture was heated to 80° C. for 2 h. The mixture was added to a sealed tube containing 4-chloro-3-iodobenzamide (230 mg, 816 μmol), tetrakis(triphenylphosphine)palladium (79 mg, 68 μmol), potassium carbonate—1.5 M in water (1.81 μl, 2.72 mmol), and ethanol (6.80 mL) and heated to 110° C. for 2 h. After cooling the reaction mixture was diluted with 75 mL of ethyl acetate, added to a separation funnel, partitioned with sodium bicarbonate (saturated, aqueous), washed 3 times with 50 mL of sodium bicarbonate (saturated, aqueous), separated, dried over sodium sulfate, concentrated in vacuo, and purified by HPLC to give the title compound. The mixture was added to a sealed tube heated to 110° C. for 2 h After cooling the reaction mixture added to a separation funnel partitioned with sodium bicarbonate (saturated, aqueous) washed 3 times with 50 mL of sodium bicarbonate (saturated, aqueous) separated dried over sodium sulfate concentrated in vacuo purified by HPLC
来源 ID: ord-ac43cb98b6b340debbd465fa1b976610反应条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-chloro-3-iodobenzoic acid (2.09 g, 7.40 mmol) was suspended in thionyl chloride (0.540 mL, 7.40 mmol) and heated to 70° C. for 3 h before it was concentrated and azeotropically dried with toluene. The concentrate was dissolved in ammonia, 0.5 M in 1,4-dioxane (92.5 mL, 37.0 mmol) to which diisopropylethylamine (6.44 mL, 37.0 mmol) was added and it was stirred at RT for 3 h. The mixture was diluted with 100 mL of ethyl acetate, added to a separation funnel, partitioned with sodium bicarbonate (saturated, aqueous), washed 4 times with 50 mL of sodium bicarbonate (saturated, aqueous), separated, dried over sodium sulfate, and concentrated in vacuo to give the title compound. MS (ES+): 282 (M+H)+. was concentrated azeotropically dried with toluene The concentrate was dissolved in ammonia added to a separation funnel partitioned with sodium bicarbonate (saturated, aqueous) washed 4 times with 50 mL of sodium bicarbonate (saturated, aqueous) separated dried over sodium sulfate concentrated in vacuo
来源 ID: ord-26595a7b65764db5be0882124cf4959c反应条件: temp:70.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-chloro-3-iodobenzoic acid (2.09 g, 7.40 mmol) was suspended in thionyl chloride (0.540 mL, 7.40 mmol) and heated to 70° C. for 3 h before it was concentrated and azeotropically dried with toluene. The concentrate was dissolved in ammonia, 0.5 M in 1,4-dioxane (92.5 mL, 37.0 mmol) to which diisopropylethylamine (6.44 mL, 37.0 mmol) was added and it was stirred at RT for 3 h. The mixture was diluted with 100 mL of ethyl acetate, added to a separation funnel, partitioned with sodium bicarbonate (saturated, aqueous), washed 4 times with 50 mL of sodium bicarbonate (saturated, aqueous), separated, dried over sodium sulfate, and concentrated in vacuo to give the title compound. MS (ES+): 282 (M+H)+. was concentrated azeotropically dried with toluene The concentrate was dissolved in ammonia added to a separation funnel partitioned with sodium bicarbonate (saturated, aqueous) washed 4 times with 50 mL of sodium bicarbonate (saturated, aqueous) separated dried over sodium sulfate concentrated in vacuo
来源 ID: ord-26595a7b65764db5be0882124cf4959cPubChem References
以下资料来自该化合物的公开数据库参考记录。
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