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HRID 1807968作成日:2026年10月23日

Acetic Acid → 5-(4-Fluoro-phenyl)-3-isopropylamino-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/ja/reaction/1807968

反応式

関与物質

役割名称HCID仕込み量
反応物Acetic AcidHCID 176—
反応物2-MethoxypropeneHCID 8300—
反応物Sodium BicarbonateHCID 516892—
反応物Methyl 3-amino-5-(4-fluorophenyl)thiophene-2-carboxylateHCID 619692—
反応物Sodium triacetoxyborohydrideHCID 5049666—
溶媒1,2-DichloroethaneHCID 11—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物5-(4-Fluoro-phenyl)-3-isopropylamino-thiophene-2-carboxylic acid methyl esterHCID 5975230191%

反応手順

To a stirred solution of 3-Amino-5-(4-fluoro-phenyl)-thiophene-2-carboxylic acid methyl ester (500 mg, 2.0 mmol) in 1,2-dichloroethane (10 mL) was added sequentially 2-methoxypropene (0.76 mL, 8.0 mmol), AcOH (0.12 mL, 4.0 mmol) and NaBH(OAc)3 (0.848 mg, 8.0 mmol) and stirred for 16 h. It was then diluted with EtOAc and H2O. The aqueous solution was adjusted to pH=7 by adding NaHCO3. The aqueous phase was extracted with EtOAc, the combined extract was washed with brine and dried on MgSO4 and filtered. Purification on bond elute with hexane to 5% EtOAc-hexane furnished 5-(4-Fluoro-phenyl)-3-isopropylamino-thiophene-2-carboxylic acid methyl ester (0.530 mg, 91% yield). 1H NMR (CDCl3, 400 MHz): δ 7.62 (d, 2H), 7.09 (m, 2H), 6.81 (s, 1H), 3.84 (s, 3H), 3.71 (m, 1H), 1.35 (d, 6H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08357718B2
出典データセットuspto-grants-2013_01
ORD IDord-cdf2aa00e00c43398a12b7b072ffe8ba
出典メモuspto-grants-2013_01