Triethylamine → HCID 90029401、化合物
反応式
[I:1][C:2]1[NH:6][N:5]=[C:4]([C:7]([NH2:9])=O)[C:3]=1[CH3:10].FC(F)(F)C(OC(=O)C(F)(F)F)=O.C(N(CC)CC)C.C(=O)(O)[O-].[Na+]>ClCCl>[I:1][C:2]1[NH:6][N:5]=[C:4]([C:7]#[N:9])[C:3]=1[CH3:10]参加物
反応条件
- 温度
- 0 °C
実験手順
Into a 100-mL round-bottom flask, was placed a solution of 5-iodo-4-methyl-1H-pyrazole-3-carboxamide (compound 258.2, 800 mg, 3.19 mmol) in dichloromethane (10 mL). The solution was cooled to 0° C., then trifluoroacetic anhydride (1.32 mL, 9.5 mmol) and triethylamine (3.16 mL, 22.7 mmol) were each added carefully drop-wise. The mixture was stirred for 2 h at 0° C., then the pH was carefully adjusted to 7-8 with aqueous sodium bicarbonate (10%). The aqueous phase was extracted with ethyl acetate (2×40 mL) and the combined organic layers were washed with 2×10 mL of brine (2×10 mL), dried (Na2SO4), filtered and concentrated under reduced pressure. The residue was purified by a silica gel chromatography with ethyl acetate/petroleum ether (1:10) as eluent to obtain the title compound as a white solid (280 mg, 38%).
後処理
- customInto a 100-mL round-bottom flask, was placed
- additioneach added carefully drop-wise
- extractionThe aqueous phase was extracted with ethyl acetate (2×40 mL)
- washthe combined organic layers were washed with 2×10 mL of brine (2×10 mL)
- dry with materialdried (Na2SO4)
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe residue was purified by a silica gel chromatography with ethyl acetate/petroleum ether (1:10) as eluent
出典と根拠
- ORDレコード
- ord-f096d29b1e60496d840a8a6b95b7be2e
- 出典データセット
- uspto-grants-2016_08
- 特許番号
- US09428502B2
反応ノート
読み込み中…