Methanamine, N-methoxy-, hydrochloride (1:1) → HCID 86697887、化合物
反応式
[F:1][C:2]1[S:6][C:5]([C:7]([OH:9])=O)=[CH:4][CH:3]=1.Cl.[CH3:11][NH:12][O:13][CH3:14].O.ON1C2C=CC=CC=2N=N1.Cl.CN(C)CCCN=C=NCC.C(N(C(C)C)CC)(C)C>O1CCCC1.O>[F:1][C:2]1[S:6][C:5]([C:7]([N:12]([O:13][CH3:14])[CH3:11])=[O:9])=[CH:4][CH:3]=1参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
To a stirred solution of 5-fluorothiophene-2-carboxylic acid (33.95 g, 232.3 mmol) in tetrahydrofuran (465 mL) at 0° C. under nitrogen is added N,O-dimethylhydroxylamine hydrochloride (45.32 g, 464.6 mmol), 1-hydroxybenzotriazole monohydrate (53.36 g, 348.5 mmol), 1-(3-dimethylaminopropyl)-3-ethylcarbodiimide hydrochloride (89.1 g, 464.6 mmol), and diisopropylethylamine (162 mL, 929 mmol). The mixture is allowed to warm to room temperature over 18 hours. The mixture is diluted with water (500 mL) and extracted with ethyl acetate (500 mL). The aqueous phase is re-extracted twice with ethyl acetate (300 mL). The combined organic extracts are dried over sodium sulfate, filtered, and concentrated under reduced pressure. The liquid residue is purified by silica gel chromatography eluting with hexanes/ethyl acetate (3:1) to give the title compound (38.28 g, 87%) as a pale yellow liquid. ES/MS (m/e): 190 (M+H).
後処理
- extractionextracted with ethyl acetate (500 mL)
- extractionThe aqueous phase is re-extracted twice with ethyl acetate (300 mL)
- dry with materialThe combined organic extracts are dried over sodium sulfate
- filtrationfiltered
- concentrationconcentrated under reduced pressure
- customThe liquid residue is purified by silica gel chromatography
- washeluting with hexanes/ethyl acetate (3:1)
出典と根拠
- ORDレコード
- ord-eac01f9b4b0a42298f65624cdf9aa3f8
- 出典データセット
- uspto-grants-2014_01
- 特許番号
- US08629270B2
反応ノート
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