反应 #4124237
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-fbdf5f27bf5b4a5a8b99d616afdde07f暂无可渲染的结构数据
C1CN(CCC1NCC2=CC=CC=C2N)CC3=CC=CC=C3中间体产品
N-[(2-aminophenyl)methyl]-1-benzylpiperidin-4-amine
结构、标识符和计算性质已按 CAS 与数据库记录完成匹配。
| 中文名称 | N-[(2-氨基苯基)甲基]-1-苄基哌啶-4-胺 |
|---|---|
| English name | N-[(2-aminophenyl)methyl]-1-benzylpiperidin-4-amine |
| IUPAC 名称 | — |
| CAS号 | 79099-03-9 |
| 数据库编号 | 13051020 |
| 分子式 | — |
| 分子量 | — |
产品信息
N-[(2-氨基苯基)甲基]-1-苄基哌啶-4-胺(CAS 79099-03-9)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 13051020
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-fbdf5f27bf5b4a5a8b99d616afdde07f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-340e915667d34cb5b9ab9ec7ca97b4be反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Then, 590 mg of 1-benzyl-4-[N-(o-aminobenzyl)amino]-piperidine, 600 mg of sulfurylamide and 12 ml of pyridine are mixed and refluxed with heating for 2 hours. The reaction mixture is cooled to room temperature and poured into 50 ml of ice water. The white crystals deposited are separated by filtration, washed with 10 ml of water and dried to obtain 520 mg of the desired product as crystals. refluxed with heating for 2 hours The white crystals deposited are separated by filtration washed with 10 ml of water dried
来源 ID: ord-e0bc648f6ef4403aaf9fa5d256bd5f38反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: In this reference example, 1.10 g of 1-benzyl-4-[N-(o-aminobenzyl)-amino]-piperidine trihydrochloride is mixed with 5 ml of water. Then, 15 ml of 1 N aqueous sodium hydroxide is added to the solution with cooling. The mixture is extracted with 20 ml of chloroform four times. The chloroform layer is washed with 20 ml of water two times. The resultant layer is dried and concentrated under reduced pressure to obtain 670 mg of 1-benzyl-4-[N-(o-aminobenzyl)amino]-piperidine as an oily residue. with cooling The mixture is extracted with 20 ml of chloroform four times The chloroform layer is washed with 20 ml of water two times The resultant layer is dried concentrated under reduced pressure
来源 ID: ord-790c3a52c56b40f8aa9a8faf8e82eb7f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-fbdf5f27bf5b4a5a8b99d616afdde07f反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-340e915667d34cb5b9ab9ec7ca97b4be反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Then, 590 mg of 1-benzyl-4-[N-(o-aminobenzyl)amino]-piperidine, 600 mg of sulfurylamide and 12 ml of pyridine are mixed and refluxed with heating for 2 hours. The reaction mixture is cooled to room temperature and poured into 50 ml of ice water. The white crystals deposited are separated by filtration, washed with 10 ml of water and dried to obtain 520 mg of the desired product as crystals. refluxed with heating for 2 hours The white crystals deposited are separated by filtration washed with 10 ml of water dried
来源 ID: ord-e0bc648f6ef4403aaf9fa5d256bd5f38反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: In this reference example, 1.10 g of 1-benzyl-4-[N-(o-aminobenzyl)-amino]-piperidine trihydrochloride is mixed with 5 ml of water. Then, 15 ml of 1 N aqueous sodium hydroxide is added to the solution with cooling. The mixture is extracted with 20 ml of chloroform four times. The chloroform layer is washed with 20 ml of water two times. The resultant layer is dried and concentrated under reduced pressure to obtain 670 mg of 1-benzyl-4-[N-(o-aminobenzyl)amino]-piperidine as an oily residue. with cooling The mixture is extracted with 20 ml of chloroform four times The chloroform layer is washed with 20 ml of water two times The resultant layer is dried concentrated under reduced pressure
来源 ID: ord-790c3a52c56b40f8aa9a8faf8e82eb7f反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of (2-amino-benzyl)-(1-benzyl-piperidin-4-yl)-amine (1.0 g, 3.39 mmol) and sulfamide (0.64 g, 6.78 mmol) in pyridine was heated at reflux for 14 h. After cooling to room temperature, the solvent was evaporated and the crude product dissolved in water. After being adjusted to pH 9 with 6N sodium hydroxide, the resulting mixture was extracted with methylene chloride (2×). The extracts were washed with water (2×), dried over sodium sulfate, filtered, and concentrated to afford an oily residue which was dissolved in ethyl acetate (4 mL). This solution was mixed with 4N HCl in 1,4-dioxane (2 mL) followed by addition of diethyl ether until precipitation of product occurred. The desired product was obtained by filtration to afford 0.7 g (53%). LC/MS: tR=0.96 min, 358.16 (MH)+. at reflux for 14 h the solvent was evaporated the crude product dissolved in water the resulting mixture was extracted with methylene chloride (2×) The extracts were washed with water (2×) dried over sodium sulfate filtered concentrated to afford an oily residue which
来源 ID: ord-f8d5b08d93664bd195095928c8a5d620反应条件: temp:60.01; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: (1-Benzyl-piperidin-4-yl)-(2-nitro-benzyl)-amine (1.2 g, 3.7 mmol) and zinc dust (1 g, excess) were combined in 75% aqueous acetic acid (16 mL) and stirred at 60° C. for 2 h. After cooling to room temperature, the solvents were removed in vacuo and the resultant crude dissolved in water (10 mL), followed by addition of ammonium hydroxide until pH 3 was attained. The solution was extracted with methylene chloride (3×). The organic layers were pooled together washed with water (2×), brine (2×), dried over sodium sulfate, filtered, and concentrated to afford 0.8 g (73%) of the desired product. 1H-NMR (CD3OD) δ 2.50 (m, 2H), 3.20 (m, 2H), 3.49 (dd, J=7.0, 7.3, 1H), 3.62 (m, 4H), 4.20 (s, 2H), 4.36 (s, 2H), 7.04 (m, 2H), 7.32 (dd, J=7.3, 7.6, 1H), 7.41 (d, J=7.9, 1H), 7.50 (m, 5H). Mass spec.: 296.40 (MH)+. After cooling to room temperature the solvents were removed in vacuo the resultant crude dissolved in water (10 mL) followed by addition of ammonium hydroxide until pH 3 The solution was extracted with methylene chloride (3×) The organic layers were pooled together washed with water (2×), brine (2×) dried over sodium sulfate filtered concentrated
来源 ID: ord-924827ea81574e8f8da1b39703ee5d4b反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of (2-amino-benzyl)-(1-benzyl-piperidin-4-yl)-amine (1.0 g, 3.39 mmol) and sulfamide (0.64 g, 6.78 mmol) in pyridine was heated at reflux for 14 h. After cooling to room temperature, the solvent was evaporated and the crude product dissolved in water. After being adjusted to pH 9 with 6N sodium hydroxide, the resulting mixture was extracted with methylene chloride (2×). The extracts were washed with water (2×), dried over sodium sulfate, filtered, and concentrated to afford an oily residue which was dissolved in ethyl acetate (4 mL). This solution was mixed with 4N HCl in 1,4-dioxane (2 mL) followed by addition of diethyl ether until precipitation of product occurred. The desired product was obtained by filtration to afford 0.7 g (53%). LC/MS: tR=0.96 min, 358.16 (MH)+. at reflux for 14 h the solvent was evaporated the crude product dissolved in water the resulting mixture was extracted with methylene chloride (2×) The extracts were washed with water (2×) dried over sodium sulfate filtered concentrated to afford an oily residue which
来源 ID: ord-1d1c4f0009244fecb3d25b8fd7b79c56反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: A solution of (2-amino-benzyl)-(1-benzyl-piperidin-4-yl)-amine (1.0 g, 3.39 mmol) and sulfamide (0.64 g, 6.78 mmol) in pyridine was heated at reflux for 14 h. After cooling to room temperature, the solvent was evaporated and the crude product dissolved in water. After being adjusted to pH 9 with 6N sodium hydroxide, the resulting mixture was extracted with methylene chloride (2×). The extracts were washed with water (2×), dried over sodium sulfate, filtered, and concentrated to afford an oily residue which was dissolved in ethyl acetate (4 mL). This solution was mixed with 4N HCl in 1,4-dioxane (2 mL) followed by addition of diethyl ether until precipitation of product occurred. The desired product was obtained by filtration to afford 0.7 g (53%). LC/MS: tR=0.96 min, 358.16 (MH)+. at reflux for 14 h the solvent was evaporated the crude product dissolved in water the resulting mixture was extracted with methylene chloride (2×) The extracts were washed with water (2×) dried over sodium sulfate filtered concentrated to afford an oily residue which
来源 ID: ord-1d1c4f0009244fecb3d25b8fd7b79c56PubChem 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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