反应 #4136188
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-d6a928b7c19f496eb1a4a25011cb8880暂无可渲染的结构数据
ClC1C=CC2=C(C=1)C=C(C)N2[H]产品信息
5-氯-2-甲基吲哚(CAS 1075-35-0)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。
可能的应用方向
仅供专业研发与工业用途
数据库编号 70636
安全提示
仅供专业研发与工业用途。操作前请依据供应商提供的安全数据表完成风险评估。
合成路线数据
12 条反应 · 12 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d6a928b7c19f496eb1a4a25011cb8880反应条件: temp:60.01; pressure:0.00; stir:
来源 ID: ord-2c33c866d4e348449996e934f2708a85反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: The sub-title compound was prepared by the method of Example 40 step a, using 5-chloro-2-methyl-1H-indole and 8-methanesulphonyl-4-chloroquinoline.
来源 ID: ord-0f7e6023f6454c3e946e32dd81ea6053反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d6a928b7c19f496eb1a4a25011cb8880反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-d6a928b7c19f496eb1a4a25011cb8880反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3,3-Dimethyl-dihydro-furan-2,5-dione (7.8 mmol, 1.0 g), 5-chloro-2-methylindole (13.8 mmol, 2.28 g), and AlCl3 (9.0 mmol, 1.2 g) were stirred in 100 mL DCE overnight at 65° C. The reaction was cooled and quenched with 10 mL water. The resultant precipitate was filtered and washed with a small amount of DCE giving 1.06 g of the sub-titled compound. The reaction was cooled quenched with 10 mL water The resultant precipitate was filtered washed with a small amount of DCE giving 1.06 g of the sub-titled compound
来源 ID: ord-fdea7c0e784241ecb857ce778f08894c反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3,3-Dimethyl-dihydro-furan-2,5-dione (7.8 mmol, 1.0 g), 5-chloro-2-methylindole (13.8 mmol, 2.28 g), and AlCl3 (9.0 mmol, 1.2 g) were stirred in 100 mL DCE overnight at 65° C. The reaction was cooled and quenched with 10 mL water. The resultant precipitate was filtered and washed with a small amount of DCE giving 1.06 g of the sub-titled compound. The reaction was cooled quenched with 10 mL water The resultant precipitate was filtered washed with a small amount of DCE giving 1.06 g of the sub-titled compound
来源 ID: ord-fdea7c0e784241ecb857ce778f08894c反应条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5-Chloro-2-methylindole (0.74 g, 2.26 mmol) and 1,4-dichloro-phthalazine (0.45 g, 2.26 mmol) were treated with 30 mL of 1,2-dichloroethane and 3.2=mmol of AlCl3 (427 mg). The resulting suspension was heated to 65° C. overnight. The reaction was cooled and quenched with 3 mL water. The resultant precipitate was filtered and dried under vacuum to give 0.65 g of the sub-title compound. MS: ESI (negative): 326, 328 (M−H). The reaction was cooled quenched with 3 mL water The resultant precipitate was filtered dried under vacuum
来源 ID: ord-41e10260748e46b5ac0bb23c2a6b50ae反应条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5-Chloro-2-methylindole (0.74 g, 2.26 mmol) and 1,4-dichloro-phthalazine (0.45 g, 2.26 mmol) were treated with 30 mL of 1,2-dichloroethane and 3.2=mmol of AlCl3 (427 mg). The resulting suspension was heated to 65° C. overnight. The reaction was cooled and quenched with 3 mL water. The resultant precipitate was filtered and dried under vacuum to give 0.65 g of the sub-title compound. MS: ESI (negative): 326, 328 (M−H). The reaction was cooled quenched with 3 mL water The resultant precipitate was filtered dried under vacuum
来源 ID: ord-41e10260748e46b5ac0bb23c2a6b50ae反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3,3-Dimethyl-dihydro-furan-2,5-dione (7.8 mmol, 1.0 g), 5-chloro-2-methylindole (13.8 mmol, 2.28 g), and AlCl3 (9.0 mmol, 1.2 g) were stirred in 100 mL DCE overnight at 65° C. The reaction was cooled and quenched with 10 mL water. The resultant precipitate was filtered and washed with a small amount of DCE giving 1.06 g of the sub-titled compound. The reaction was cooled quenched with 10 mL water The resultant precipitate was filtered washed with a small amount of DCE giving 1.06 g of the sub-titled compound
来源 ID: ord-7c5e951ea48447a3bd7b0672c648a2e7反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 3,3-Dimethyl-dihydro-furan-2,5-dione (7.8 mmol, 1.0 g), 5-chloro-2-methylindole (13.8 mmol, 2.28 g), and AlCl3 (9.0 mmol, 1.2 g) were stirred in 100 mL DCE overnight at 65° C. The reaction was cooled and quenched with 10 mL water. The resultant precipitate was filtered and washed with a small amount of DCE giving 1.06 g of the sub-titled compound. The reaction was cooled quenched with 10 mL water The resultant precipitate was filtered washed with a small amount of DCE giving 1.06 g of the sub-titled compound
来源 ID: ord-7c5e951ea48447a3bd7b0672c648a2e7反应条件: temp:65.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: 5-Chloro-2-methylindole (0.74 g, 2.26 mmol) and 1,4-dichloro-phthalazine (0.45 g, 2.26 mmol) were treated with 30 mL of 1,2-dichloroethane and 3.2 mmol of AlCl3 (427 mg). The resulting suspension was heated to 65° C. overnight. The reaction was cooled and quenched with 3 mL water. The resultant precipitate was filtered and dried under vacuum to give 0.65 g of the sub-title compound. MS: ESI (negative): 326, 328 (M−H). The reaction was cooled quenched with 3 mL water The resultant precipitate was filtered dried under vacuum
来源 ID: ord-6599291c2ae44f3da0ff32935552d507PubChem References
以下资料来自该化合物的公开数据库参考记录。
