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HRID 348498Erstellt: 25. Oktober 2026

3-Thiophenamine, tetrahydro-, 1,1-dioxide → 4-(1,1-Dioxotetrahydrothiophen-3-ylamino)-2-methylsulfanylpyrimidine-5-carboxylic acid (4-fluorophenyl)amide

https://huagongshe.com/reaction/348498

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-Thiophenamine, tetrahydro-, 1,1-dioxideHCID 22807—
EduktDiisopropylethylamineHCID 81531—
Edukt4-Chloro-2-methylsulfanylpyrimidine-5-carboxylic acid (4-fluorophenyl)amideHCID 18858805—
LösungsmittelMethanolHCID 887—
Produkt4-(1,1-Dioxotetrahydrothiophen-3-ylamino)-2-methylsulfanylpyrimidine-5-carboxylic acid (4-fluorophenyl)amideHCID 8676040355,2%

Reaktionsschritte

To a suspension of 3-amino-1,1-dioxotetrahydrothiophene (345 mg, 2.01 mmol) in methanol (5 mL) was added DIPEA (350 μL) followed by 4-chloro-2-methylsulfanylpyrimidine-5-carboxylic acid (4-fluorophenyl)amide (200 mg, 0.67 mmol). The mixture was allowed to stir for 16 h. The resulting mixture was poured into ice-water and the resulting solids were collected by filtration. The solids were washed with ethyl acetate and hexanes and were dried. This afforded 147 mg (0.37 mmol, 55% yield) of the titled product as a solid. 1H NMR (300 MHz, DMSO-d6) δ 10.25 (s, 1H), 8.78 (d, 1H), 8.65 (s, 1H), 7.65 (m, 2H), 7.18 (m, 2H), 4.87 (m, 1H), 3.52 (m, 1H), 3.35–3.04 (m, 3H), 2.50, M, 1H), 2.22 (m, 1H); MS (EI) m/z 395.05 (M−H)−.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07176310B1
Quelldatensatzuspto-grants-2007_02
ORD IDord-9a4e01f6a8ea4770a3f348bda284ba12
Quellennotizuspto-grants-2007_02