反应 #4040421
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-d979656c3a384093a8cbad5bea169e01暂无可渲染的结构数据
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N-异丙基-1-哌啶乙酰胺(CAS 39890-42-1)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-d979656c3a384093a8cbad5bea169e01反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-054ef913402f444099a352b50b42dbfc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-bcdf4d2dd473485e8629de4dd0fd2600反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-{1-[5-chloro-2-(trifluoromethyl)benzyl]-1,2,3,4-tetrahydropyrido[2,3-b]pyrazin-7-yl}benzoic acid was reacted with 2-piperazinyl-N-isopropylacetamide as in General Procedure 10 to give the title compound. LCMS: m/z=615.03 (M+H+); retention time=0.58 minutes.
来源 ID: ord-3a50cbff496b4109b0469c0dec2573b6反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3-{1-[5-chloro-2-(trifluoromethyl)benzyl]-1,2,3,4-tetrahydropyrido[2,3-b]pyrazin-7-yl}benzoic acid was reacted with 2-piperazinyl-N-isopropylacetamide as in General Procedure 10 to give the title compound. LCMS: m/z=615.01 (M+H+); retention time=0.61 minutes.
来源 ID: ord-3a207540183d481a899c76c21b9ed83c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3-{1-[5-chloro-2-(trifluoromethyl)benzyl]-1,2,3,4-tetrahydropyrido[2,3-b]pyrazin-7-yl}benzoic acid was reacted with 2-piperazinyl-N-isopropylacetamide as in General Procedure 10 to give the title compound. LCMS: m/z=615.01 (M+H+); retention time=0.61 minutes.
来源 ID: ord-3a207540183d481a899c76c21b9ed83c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 4.6 g of anisic acid chloride in 20 ml of methylene chloride is added dropwise to 5 g of piperazinoacetic acid isopropylamide in 20 ml of methylene chloride at 0° C. The mixture is then stirred at room temperature for 4 hours and subsequently concentrated. The residue is recrystallised from isopropanol. subsequently concentrated The residue is recrystallised from isopropanol
来源 ID: ord-8c3022f585c949368e9772787e8e09b8反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d979656c3a384093a8cbad5bea169e01反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of 4.6 g of anisic acid chloride in 20 ml of methylene chloride is added dropwise to 5 g of piperazinoacetic acid isopropylamide in 20 ml of methylene chloride at 0° C. The mixture is then stirred at room temperature for 4 hours and subsequently concentrated. The residue is recrystallised from isopropanol. subsequently concentrated The residue is recrystallised from isopropanol
来源 ID: ord-8c3022f585c949368e9772787e8e09b8反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-054ef913402f444099a352b50b42dbfc反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-bcdf4d2dd473485e8629de4dd0fd2600反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The crude product obtained using (E)-4-[2-(1H-indazol-3-yl)vinyl]benzoic acid (200 mg, 0.757 mmol) obtained in Step 6 of Example 1, N-methylmorpholine (0.166 mL, 1.51 mmol), 1-ethyl-3-(3-dimethylaminopropyl)carbodiimide hydrochloride (203 mg, 1.06 mmol), 1-hydroxybenzotriazole monohydrate (133 mg, 0.984 mmol) and-N-isopropyl-2-(piperazin-1-yl)acetamide (210 mg, 1.14 mmol) in a similar manner to Step 7 of Example 1, was purified by silica gel column chromatography (chloroform/methanol=80/20), followed by treating with 4 mol/L hydrogen chloride-ethyl acetate solution (0.665 mL) to obtain Compound 135 (99.7 mg, 26%).
来源 ID: ord-bccc0877d9654120ab336e6d83216bcbPubChem References
以下资料来自该化合物的公开数据库参考记录。
