反応式
[N+:1]([C:4]1[CH:5]=[N:6][NH:7][CH:8]=1)([O-])=O.C(=O)([O-])[O-].[Cs+].[Cs+].[CH2:15]1[O:18][C@@H:16]1[CH3:17]>>[NH2:1][C:4]1[CH:5]=[N:6][N:7]([CH2:15][C@H:16]([OH:18])[CH3:17])[CH:8]=1参加物
実験手順
To a solution of 4-nitropyrazole (44.7 mg, 0.395 mmol, 1 equiv) in (R)-propylene oxide (1 mL) was added cesium carbonate (78 mg, 0.24 mmol, 0.61 equiv) at 24° C. After 64 h, the reaction mixture was partitioned between ethyl acetate (3 mL) and half-saturated aqueous sodium chloride solution (3 mL). The organic was separated, and the remaining aqueous phase was extracted with ethyl acetate (2×3 mL). The collected organic was dried over anhydrous sodium sulfate, filtered, and concentrated. The resulting residue was dissolved in methanol (4 mL) and circulated through a H-Cube® continuous-flow hydrogenation reactor (ThalesNano) fitted with a palladium on carbon catalyst cartridge at 30° C. The resulting solution was concentrated in vacuo to provide product as a pink oil, which was used without further purification. 1H NMR (500 MHz, CDCl3), δ: 7.17 (s, 1H), 7.01 (s, 1H), 4.13 (m, 1H), 4.00 (dd, J=13.8, 2.7 Hz, 1H), 3.84 (dd, J=13.8, 7.9 Hz, 1H), 3.47 (s, 1H), 3.15 (br s, 2H), 1.18 (d, J=6.3 Hz, 3H).
後処理
- customthe reaction mixture was partitioned between ethyl acetate (3 mL) and half-saturated aqueous sodium chloride solution (3 mL)
- customThe organic was separated
- extractionthe remaining aqueous phase was extracted with ethyl acetate (2×3 mL)
- dry with materialThe collected organic was dried over anhydrous sodium sulfate
- filtrationfiltered
- concentrationconcentrated
- dissolutionThe resulting residue was dissolved in methanol (4 mL)
- customfitted with a palladium on carbon catalyst cartridge at 30° C
- concentrationThe resulting solution was concentrated in vacuo
- customto provide product as a pink oil, which
- customwas used without further purification
出典と根拠
- ORDレコード
- ord-4df50af20b264787b9a064f695406e95
- 出典データセット
- uspto-grants-2016_09
- 特許番号
- US09434732B2
関連ノート
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