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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411208Generated: October 27, 2026

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

https://huagongshe.com/reaction/411208

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) δ 3.78, 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 numberUS06559145B2
Source datasetuspto-grants-2003_05
ORD IDord-dbe59273da13454c960eff6e2169e250
Source noteuspto-grants-2003_05