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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 73165Erstellt: 23. Oktober 2026

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

https://huagongshe.com/de/reaction/73165

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
Edukt2-MethoxypropeneHCID 8300—
EduktSodium BicarbonateHCID 516892—
EduktMethyl 3-amino-5-(4-fluorophenyl)thiophene-2-carboxylateHCID 619692—
EduktSodium triacetoxyborohydrideHCID 5049666—
Lösungsmittel1,2-DichloroethaneHCID 11—
LösungsmittelWaterHCID 962—
LösungsmittelEthyl AcetateHCID 8857—
Produkt5-(4-Fluoro-phenyl)-3-isopropylamino-thiophene-2-carboxylic acid methyl esterHCID 5975230191%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829030B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-5bd717609296450abc7645a50104cf74
Quellennotizuspto-grants-2014_09