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HRID 1070624Erstellt: 26. Oktober 2026

Triethylamine → 2-(4-Morpholinylcarbonyl)-1,3-thiazol-5-amine

https://huagongshe.com/reaction/1070624

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
EduktAminoacetonitrile sulfate (1:1)HCID 196971—
EduktMethyl 4-morpholinyl(oxo)ethanedithioateHCID 22397235—
LösungsmittelMethanolHCID 887—
Produkt2-(4-Morpholinylcarbonyl)-1,3-thiazol-5-amineHCID 2239722631%

Reaktionsschritte

To a stirring mixture of methyl 4-morpholinyl(oxo)ethanedithioate (Preparation 25, 500 mg) and aminoacetonitrile bisulfate (564 mg) in MeOH (10 mL) at 0° C. is added triethylamine in MeOH (5 mL). The mixture is stirred overnight and allowed to warm to ambient temperature. The solution is filtered, and solvent removed from the filtrate. The residue is washed with water (15 mL) and extracted with EtOAc (3×20 mL), dried over MgSO4, and the solvent removed. The residue is purified by SiO2 flash column chromatography (eluent 3/1 EtOAc/hexane) to afford 161 mg (31%) of the title compound as a light brown solid. Physical characteristics: 1H NMR (CDCl3) δ3.78, 4.35, 7.05; IR (diffuse reflectance) 3321, 3217, 2858, 1580, 1438, 1418, 1348, 1276, 1178, 1113, 1003, 834, 783, 731, 619 cm−1; MS (ESI+) m/z 214 (M+H)+. Anal. Found: C, 45.24; H, 5.33; N, 19.42.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06903097B2
Quelldatensatzuspto-grants-2005_06
ORD IDord-8b5410d9198848f39eb671481d19ace6
Quellennotizuspto-grants-2005_06