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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1807997Erstellt: 24. Oktober 2026

Acetic Acid → 3-(1-Methyl-piperidin-4-ylamino)-5-phenyl-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/de/reaction/1807997

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetic AcidHCID 176—
EduktSodium HydroxideHCID 14798—
EduktMethyl 3-amino-5-phenylthiophene-2-carboxylateHCID 700562—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt1-Methyl-4-trimethylsilanyloxy-1,2,3,6-tetrahydro-pyridineHCID 10081120—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt3-(1-Methyl-piperidin-4-ylamino)-5-phenyl-thiophene-2-carboxylic acid methyl esterHCID 2077574973%

Reaktionsschritte

To a stirred solution of methyl-3-amino-5-phenylthiophene-carboxylate (233 mg, 1.0 mmol) and 1-methyl-4-trimethylsilanyloxy-1,2,3,6-tetrahydro-pyridine (370 mg, 2.0 mmol) in dichloroethane (3.0 mL) was added AcOH (0.114 mL, 2.0 eq) and followed addition of NaBH(OAc)3 (424 mg, 2.0 mmol) in one portion. The resultant reaction mixture was stirred at RT for weekend, aq. 10% NaOH (until basic) was added, after 30 min, reaction mixture was extracted with dichloromethane. The organic extract was washed with brine and dried. The crude product was purified on silica gel column using 20% EtOAc/hexane for unreacted starting material followed by CHCl3/MeOH/Et3N (180/16/1) furnished the 3-(1-methyl-piperidin-4-ylamino)-5-phenyl-thiophene-2-carboxylic acid methyl ester (240 mg, 73%). NMR 1H (CDCl3, 400 MHz): 7.64-7.6 (m, 2H), 7.43-7.34 (m, 3H), 6.83 (brs, 2H), 3.83 (s, 3H), 3.46-3.4 (m, 1H), 2.82-2.74 (m, 1H), 2.3 (s, 3H), 2.26-2.2 (m, 4H), 1.72-1.62 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08357718B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-8c539e10f72a412ebbcd3e3476afcca5
Quellennotizuspto-grants-2013_01