反应 #4132524
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-d4c8643ed9bf4c34b20ac7be2d9ab5b4暂无可渲染的结构数据
FC1=C(C=CC2=C1C=C(C)N2)N产品信息
5-氨基-4-氟-2-甲基吲哚(CAS 398487-76-8)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-d4c8643ed9bf4c34b20ac7be2d9ab5b4反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d4c8643ed9bf4c34b20ac7be2d9ab5b4反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-Fluoro-2-methyl-5-phthalimidoindole (1.2, 4 mmol) was dissolved in methanol (30 ml). Hydrazine monohydrate (260 μl, 5.3 mmol) was added and the reaction mixture was stirred at ambient temperature for 2 hours. The solvent was evaporated off and the residue taken up in methylene chloride. The phthalhydrazide by-product was removed by filtration and the filtrate purified by flash chromatography 0.5% methanol in methylene chloride. Evaporation of the solvent gave a white solid which contained traces of phthalhydrazide. Further purification was done by dissolving it in ethyl acetate, washing the organic phase with NaOH 2N and brine, drying over MgSO4. Rotary evaporation of the solvent gave 5-amino-4-fluoro-2-methylindole (500 mg, 76%). The solvent was evaporated off The phthalhydrazide by-product was removed by filtration the filtrate purified by flash chromatography 0.5% methanol in methylene chloride Evaporation of the solvent gave a white solid which Further purification by dissolving it in ethyl acetate washing the organic phase with NaOH 2N and brine drying over MgSO4 Rotary evaporation of the solvent
来源 ID: ord-009fa7e715004d1cb4ad344c5eb8e5d9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-Fluoro-2-methyl-5-phthalimidoindole (1.2, 4 mmol) was dissolved in methanol (30 ml). Hydrazine monohydrate (260 μl, 5.3 mmol) was added and the reaction mixture was stirred at ambient temperature for 2 hours. The solvent was evaporated off and the residue taken up in methylene chloride. The phthalhydrazide by-product was removed by filtration and the filtrate purified by flash chromatography 0.5% methanol in methylene chloride. Evaporation of the solvent gave a white solid which contained traces of phthalhydrazide. Further purification was done by dissolving it in ethyl acetate, washing the organic phase with NaOH 2N and brine, drying over MgSO4. Rotary evaporation of the solvent gave 5-amino-4-fluoro-2-methylindole (500 mg, 76%). The solvent was evaporated off The phthalhydrazide by-product was removed by filtration the filtrate purified by flash chromatography 0.5% methanol in methylene chloride Evaporation of the solvent gave a white solid which Further purification by dissolving it in ethyl acetate washing the organic phase with NaOH 2N and brine drying over MgSO4 Rotary evaporation of the solvent
来源 ID: ord-009fa7e715004d1cb4ad344c5eb8e5d9反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 4-Fluoro-2-methyl-5-phthalimidoindole (1.2, 4 mmol) was dissolved in methanol (30 ml). Hydrazine monohydrate (260 μl, 5.3 mmol) was added and the reaction mixture was stirred at ambient temperature for 2 hours. The solvent was evaporated off and the residue taken up in methylene chloride. The phthalhydrazide by-product was removed by filtration and the filtrate purified by flash chromatography 0.5% methanol in methylene chloride. Evaporation of the solvent gave a white solid which contained traces of phthalhydrazide. Further purification was done by dissolving it in ethyl acetate, washing the organic phase with NaOH 2N and brine, drying over MgSO4. Rotary evaporation of the solvent gave 5-amino-4-fluoro-2-methylindole (500 mg, 76%). The solvent was evaporated off The phthalhydrazide by-product was removed by filtration the filtrate purified by flash chromatography 0.5% methanol in methylene chloride Evaporation of the solvent gave a white solid which Further purification by dissolving it in ethyl acetate washing the organic phase with NaOH 2N and brine drying over MgSO4 Rotary evaporation of the solvent
来源 ID: ord-009fa7e715004d1cb4ad344c5eb8e5d9PubChem References
以下资料来自该化合物的公开数据库参考记录。
