Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 73205Erstellt: 23. Oktober 2026

Phenylsilane → 5-Phenyl-3-(tetrahydro-thiopyran-4-ylamino)-thiophene-2-carboxylic acid methyl ester

https://huagongshe.com/de/reaction/73205

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktPhenylsilaneHCID 12752—
EduktTetrahydrothiopyran-4-oneHCID 66173—
EduktMethyl 3-amino-5-phenylthiophene-2-carboxylateHCID 700562—
KatalysatorDibutyltin dichlorideHCID 12688—
LösungsmittelTetrahydrofuranHCID 8028—
Produkt5-Phenyl-3-(tetrahydro-thiopyran-4-ylamino)-thiophene-2-carboxylic acid methyl esterHCID 5975237456,5%

Reaktionsschritte

Reductive amination of 3-amino-5-phenyl-thiophene-2-carboxylic acid methyl ester (0.933 g, 4.0 mmol) and tetrahydro-thiopyran-4-one (0.464 g, 4.0 mmol) in THF (1.0 mL) employing Bu2SnCl2 (60.5 mg, 0.2 mmol) and PhSiH3 (0.476 g, 0.542 mL) was carried out as described for example 13, step 1 gave 5-phenyl-3-(tetrahydro-thiopyran-4-ylamino)-thiophene-2-carboxylic acid methyl ester (0.753 g, 56.3%). NMR 1H (CDCl3, 400 MHz): 7.64-7.6 (m, 2H), 7.44-7.34 (m, 3H), 6.9 (brm, 1H), 6.81 (brs, 1H), 3.84 (s, 3H), 3.5-3.4 (m, 1H), 2.85-2.7 (m, 4H), 2.4-2.25 (m, 2H), 1.85-1.7 (m, 2H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08829030B2
Quelldatensatzuspto-grants-2014_09
ORD IDord-9887b9a5d4de4344accb803ab0a9f125
Quellennotizuspto-grants-2014_09