反応式
[Cl-].[NH4+].[CH3:3][C:4]1[C:9]([N+:10]([O-])=O)=[CH:8][CH:7]=[C:6]([N:13]2[CH:17]=[N:16][CH:15]=[N:14]2)[N:5]=1>C(OCC)(=O)C.[Zn]>[CH3:3][C:4]1[C:9]([NH2:10])=[CH:8][CH:7]=[C:6]([N:13]2[CH:17]=[N:16][CH:15]=[N:14]2)[N:5]=1参加物
反応条件
- 温度
- 0 °C
実験手順
A mixture of zinc (Aldrich, <10 micron; 798 mg, 12.2 mmol) in aqueous ammonium chloride (2 M; 6.1 mL, 12.2 mmol) was cooled to 0° C. using an ice-water bath, and stirred at this temperature for 15 min. A solution of 2-methyl-3-nitro-6-[1,2,4]triazol-1-yl-pyridine (500 mg, 2.44 mmol) in ethyl acetate (8 mL) was added and the mixture was stirred at 0° C. for 1 h and then at room temperature overnight. The mixture was then filtered through Celite™ to remove zinc dust, and the Celite™ was washed with ethyl acetate and methanol. Water and ethyl acetate were added to the filtrate and the mixture was shaken and then filtered to remove some solid material between the two layers. The aqueous layer was extracted twice with ethyl acetate and the combined organic layers were evaporated to dryness under high vacuum to give 2-methyl-6-[1,2,4]triazol-1-yl-pyridin-3-ylamine (322 mg, 75%) as a yellow solid. 1H NMR (300 MHz, DMSO-d6) δ 2.30 (s, 3H), 5.37 (s, 2H), 7.11 (d, 1H, J=8.4 Hz), 7.38 (d, 1H, J=8.4 Hz), 8.13 (s, 1H), 9.03 (s, 1H).
後処理
- stirringthe mixture was stirred at 0° C. for 1 h
- customat room temperature
- customovernight
- filtrationThe mixture was then filtered through Celite™
- customto remove zinc dust
- washthe Celite™ was washed with ethyl acetate and methanol
- additionWater and ethyl acetate were added to the filtrate
- stirringthe mixture was shaken
- filtrationfiltered
- customto remove some solid material between the two layers
- extractionThe aqueous layer was extracted twice with ethyl acetate
- customthe combined organic layers were evaporated to dryness under high vacuum
出典と根拠
- ORDレコード
- ord-ea458cd4434d4d14b4e836102b8328cd
- 出典データセット
- uspto-grants-2012_05
- 特許番号
- US08188098B2
関連ノート
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