反应 #4046741
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-370f0b5b6f9b443ba4305b0d23a76e5e暂无可渲染的结构数据
C1CC1CN2CCC(CC2)O产品信息
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8 条反应 · 8 篇文献
反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-370f0b5b6f9b443ba4305b0d23a76e5e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-706442e65c3a452fab76cb761c3cbd16反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a cold (0° C.) solution of 1-cyclopropylmethyl-piperidin-4-one (314 mg, 2 mmol, 1.0 eq.) in ethanol (4 mL) was added sodium borohydride (61 mg, 2 mmol, 0.75 eq.). The reaction mixture was stirred 16 h at room temperature. Water, sodium hydroxide and dichloromethane were added and the reaction mixture was stirred 2 h at room temperature. The aqueous layer was extracted with dichloromethane and the combined organic phases were dried over sodium sulfate, filtered then concentrated to dryness in vacuo to yield 160 mg (50%) of the tide compound as colorless oil, witch was used in the next step without further purification. MS (m/e): 156.3 (MH+, 100%). the reaction mixture was stirred 2 h at room temperature The aqueous layer was extracted with dichloromethane the combined organic phases were dried over sodium sulfate filtered then concentrated to dryness in vacuo
来源 ID: ord-e5dc8ef68c4e4b3b899fcdc442eaa797反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-370f0b5b6f9b443ba4305b0d23a76e5e反应条件: temp:0.00; pressure:0.00; stir:
来源 ID: ord-706442e65c3a452fab76cb761c3cbd16反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Add NaH (60% dispersion in oil, 130 mg, 3.25 mmol) to a solution of 1-cyclopropylmethyl-piperidin-4-ol (preparation 11, 458 mg, 2.95 mmol) in DMF (8 mL) and stir for 20 min. Then add 2,6-dichloropyridine to the mixture and heat at 120° C. overnight. Quench the reaction with saturated NaHCO3, extract with methylene dichloride three times. Combine the organic layers, wash with saturated NaCl solution, dry over Na2SO4, filter and concentrate to give a residue. Chromatography (silica gel) eluting with 4% 2M NH3-methanol in methylene dichloride provides 480 mg (61%) of the title compound: mass spectrum (ion spray): m/z=267.2 (M+1); 1H NMR (CDCl3, ppm): 7.39 (t, 1H), 6.75 (d, 1H), 6.52 (d, 1H), 4.96 (m, 1H), 2.75 (m, 2H), 2.30 (m, 2H), 2.19 (d, 2H), 1.97 (m, 2H), 1.75 (m, 2H), 0.76 (m, 1H), 0.43 (m, 2H), 0.00 (m, 2H). Quench the reaction with saturated NaHCO3 extract with methylene dichloride three times Combine the organic layers, wash with saturated NaCl solution dry over Na2SO4 filter concentrate to give a residue Chromatography (silica gel) eluting with 4% 2M NH3-methanol in methylene dichloride
来源 ID: ord-9cef1e8696f9412d89afe1c9b59298c5反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: Add bromomethylcyclopropane (2.025 g, 15 mmol) to a solution of 4-hydroxypiperidine (3.035 g, 30 mmol) in THF (10 mL) and stir the mixture overnight. Dilute the mixture with ethylacetate, wash with saturated NaHCO3 solution, dry over Na2SO4, filter and concentrate to give a residue. Chromatography (silica gel, eluting with 8% 2M NH3-methanol in CH2Cl2) provides 1.087 g (47%) of the title compound: mass spectrum (ion spray): m/z=156.2 (M+1); 1H NMR (CDCl3, ppm): 3.60 (m, 1H), 2.81 (m, 2H), 2.16 (d, 1H), 2.10 (m, 3H), 1.84 (m, 2H), 1.53 (m, 3H), 0.79 (m, 1H), 0.44 (m, 2H), 0.00 (m, 2H). wash with saturated NaHCO3 solution dry over Na2SO4 filter concentrate to give a residue Chromatography (silica gel, eluting with 8% 2M NH3-methanol in CH2Cl2)
来源 ID: ord-477683910d6f4a09a72aa1c87f311dca反应条件: temp:0.00; pressure:0.00; stir:; See reaction.notes.procedure_details.
实验步骤: To a cold (0° C.) solution of 1-cyclopropylmethyl-piperidin-4-one (314 mg, 2 mmol, 1.0 eq.) in ethanol (4 mL) was added sodium borohydride (61 mg, 2 mmol, 0.75 eq.). The reaction mixture was stirred 16 h at room temperature. Water, sodium hydroxide and dichloromethane were added and the reaction mixture was stirred 2 h at room temperature. The aqueous layer was extracted with dichloromethane and the combined organic phases were dried over sodium sulfate, filtered then concentrated to dryness in vacuo to yield 160 mg (50%) of the tide compound as colorless oil, witch was used in the next step without further purification. MS (m/e): 156.3 (MH+, 100%). the reaction mixture was stirred 2 h at room temperature The aqueous layer was extracted with dichloromethane the combined organic phases were dried over sodium sulfate filtered then concentrated to dryness in vacuo
来源 ID: ord-e5dc8ef68c4e4b3b899fcdc442eaa797PubChem References
以下资料来自该化合物的公开数据库参考记录。
