反应 #4056940
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-5ead01cda05446718370877eafcec653暂无可渲染的结构数据
C1C(C1F)N产品信息
2-氟环丙烷-1-胺(CAS 143062-83-3)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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合成路线数据
6 条反应 · 6 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5ead01cda05446718370877eafcec653反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-87292787e56b408691ae2f1755a99c44反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-5ead01cda05446718370877eafcec653反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: As for the method for producing the starting materials, an example for the preparation of the compound (IIa) is described below: ##STR7## That is, ethyl 3-ethoxy-2-(2,4,5-trifluorobenzoyl)acrylate (VIa; R4 =C2H5) is reacted with 1-amino-2-fluorocyclopropane (or an acid addition salt thereof such as trifluoroacetate in the presence of at least a molar equivalent of a proper base such as triethylamine), and the resulting ethyl 3-(cis-2-fluorocyclopropyl)amino-2-(2,4,5-trifluorobenzoyl)acrylate (VIIa; R4 =C2H5) can be reacted with approximately a molar equivalent of sodium hydride in a solvent such as anhydrous dioxane at a temperature of from 20° C. to 50° C. to yield ethyl 1-(2-fluorocyclopropyl)-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate (IIa; R4 =C2H5) in good yield. As for the method for producing the starting materials an acid addition salt
来源 ID: ord-d651faecf4da4578beb1ac180e549288反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: As for the method for producing the starting materials, an example for the preparation of the compound (IIa) is described below: ##STR7## That is, ethyl 3-ethoxy-2-(2,4,5-trifluorobenzoyl)acrylate (VIa; R4 =C2H5) is reacted with 1-amino-2-fluorocyclopropane (or an acid addition salt thereof such as trifluoroacetate in the presence of at least a molar equivalent of a proper base such as triethylamine), and the resulting ethyl 3-(cis-2-fluorocyclopropyl)amino-2-(2,4,5-trifluorobenzoyl)acrylate (VIIa; R4 =C2H5) can be reacted with approximately a molar equivalent of sodium hydride in a solvent such as anhydrous dioxane at a temperature of from 20° C. to 50° C. to yield ethyl 1-(2-fluorocyclopropyl)-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate (IIa; R4 =C2H5) in good yield. As for the method for producing the starting materials an acid addition salt
来源 ID: ord-d651faecf4da4578beb1ac180e549288反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: As for the method for producing the starting materials, an example for the preparation of the compound (IIa) is described below: ##STR7## That is, ethyl 3-ethoxy-2-(2,4,5-trifluorobenzoyl)acrylate (VIa; R4 =C2H5) is reacted with 1-amino-2-fluorocyclopropane (or an acid addition salt thereof such as trifluoroacetate in the presence of at least a molar equivalent of a proper base such as triethylamine), and the resulting ethyl 3-(cis-2-fluorocyclopropyl)amino-2-(2,4,5-trifluorobenzoyl)acrylate (VIIa; R4 =C2H5) can be reacted with approximately a molar equivalent of sodium hydride in a solvent such as anhydrous dioxane at a temperature of from 20° C. to 50° C. to yield ethyl 1-(2-fluorocyclopropyl)-6,7-difluoro-1,4-dihydro-4-oxoquinoline-3-carboxylate (IIa; R4 =C2H5) in good yield. As for the method for producing the starting materials an acid addition salt
来源 ID: ord-d651faecf4da4578beb1ac180e549288PubChem 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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