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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070624Generated: October 25, 2026

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

https://huagongshe.com/reaction/1070624

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantAminoacetonitrile sulfate (1:1)HCID 196971—
ReactantMethyl 4-morpholinyl(oxo)ethanedithioateHCID 22397235—
SolventMethanolHCID 887—
Product2-(4-Morpholinylcarbonyl)-1,3-thiazol-5-amineHCID 2239722631%

Reaction Steps

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.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903097B2
Source datasetuspto-grants-2005_06
ORD IDord-8b5410d9198848f39eb671481d19ace6
Source noteuspto-grants-2005_06