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HRID 1770938Erstellt: 25. Oktober 2026

2-Oxopropanethioamide → 6'-Bromo-4-methoxy-5''-methyl-3'H-dispiro[cyclohexane-1,2'-indene-1',2''-imidazole]-4''(3''H)-thione

https://huagongshe.com/reaction/1770938

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2-OxopropanethioamideHCID 20765237—
EduktTrans-6'-bromo-4-methoxyspiro[cyclohexane-1,2'-inden]-1'(3'H)-imineHCID 67979447—
LösungsmittelMethanolHCID 887—
Produkt6'-Bromo-4-methoxy-5''-methyl-3'H-dispiro[cyclohexane-1,2'-indene-1',2''-imidazole]-4''(3''H)-thioneHCID 8666727164,5%

Reaktionsbedingungen

Temperatur60 °C

Reaktionsschritte

6′-Bromo-4-methoxyspiro[cyclohexane-1,2′-inden]-1′(3′H)-imine (Example 19 Step 2, 1.41 g, 4.57 mmol) and 2-oxopropanethioamide (Intermediate 2, 1.42 g, 13.7 mmol) were dissolved in dry MeOH (30 mL) and the resulting solution was heated at 60° C. under an atmosphere of nitrogen. After 15 h the reaction was allowed to cool to r.t. A precipitate had formed which was filtered off and dried in vacuo, yielding the title compound (1.16 g, 64% yield) as a mixture of isomers. 1H NMR (500 MHz, DMSO-d6) δ ppm 1.18 (m, 4H), 1.47 (m, 2H), 1.87 (m, 2H), 2.27 (m, 3H), 3.03 (m, 3H), 3.20 (s, 3H), 6.98 (d, 1H), 7.34 (d, 1H), 7.51 (dd, 1H); MS (APCI+) m/z 394 [M+H]+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09248129B2
Quelldatensatzuspto-grants-2016_02
ORD IDord-f235d13388f34623bbe0517029c2ce6a
Quellennotizuspto-grants-2016_02