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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 411211Generated: October 25, 2026

Methyl iodide → Diethyl 2-((Methyl(2-(morpholin-4-ylmethyl)-1,3-thiazol-5-yl)amino)methylene)-malonate

https://huagongshe.com/reaction/411211

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
ReactantPotassium CarbonateHCID 11430—
ReactantDiethyl 2-(((2-(Morpholin-4-ylmethyl)-1,3-thiazol-5-yl)amino)methylene)malonateHCID 22397215—
SolventDimethylformamideHCID 6228—
ProductDiethyl 2-((Methyl(2-(morpholin-4-ylmethyl)-1,3-thiazol-5-yl)amino)methylene)-malonateHCID 2239717763%

Reaction Conditions

Temperature75 °C

Reaction Steps

To a mixture of diethyl 2-(((2-(morpholin4-ylmethyl)-1,3-thiazol-5-yl)amino)-methylene)malonate (Preparation 28, 1.51 g) and K2CO3 (1.19 g) in DMF (15 mL) at ambient temperature is added iodomethane (0.28 mL). The mixture is heated to 75° C. in a sealed pressure tube and stirred overnight. The solution is cooled to ambient temperature and the solvent is removed. The mixture is diluted with water (75 mL) and extracted with EtOAc (3×75 mL). The organic layer is dried (MgSO4) and the solvent removed to afford 0.984 g (63%) of the title compound as a light brown solid. Physical characteristics: 1H NMR (CDCl3) δ 1.24-1.33, 2.60, 3.31, 3.74, 4.17-4.24, 7.60; IR (liq.) 1702, 1608, 1535, 1453, 1383, 1365, 1293, 1270, 1232, 1206, 1117, 1096, 1071, 1010, 865 cm−1; HRMS (FAB) m/z 384.1600 (C17H25N3O5S+H). Anal. Found: C, 53.18; H, 6.64; N, 10.41.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06559145B2
Source datasetuspto-grants-2003_05
ORD IDord-c8911d34df0148a4b1e85043b88d114b
Source noteuspto-grants-2003_05