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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 479703Generated: November 3, 2026

Ethyl Acetate → 1-[2-(3-Methoxyphenyl)thiazol-4-yl]-3-(6-piperidin-1-ylmethyl-pyridin-2-yl)urea

https://huagongshe.com/reaction/479703

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantDiphenylphosphoryl azideHCID 123414—
Reactant2-(3-Methoxyphenyl)-1,3-thiazole-4-carboxylic acidHCID 15623065—
Reactant2-Amino-6-(piperidin-1-ylmethyl)pyridineHCID 18771671—
SolventTolueneHCID 1140—
Product1-[2-(3-Methoxyphenyl)thiazol-4-yl]-3-(6-piperidin-1-ylmethyl-pyridin-2-yl)ureaHCID 18771802—

Reaction Conditions

Temperature85 °C

Reaction Steps

To a stirred solution of 2-(3-methoxyphenyl)-1,3-thiazole-4-carboxylic acid (0.17 g, 0.72 mmol) in toluene (10 mL) at RT and under N2 was added TEA (0.2 mL). After 5 min, (PhO)2PON3 (0.2 5 mL) was added and the reaction mixture was heated at 85° C. for 20 min followed by the addition of 6-(piperidylmethyl)-2-pyridylamine (0.21 g, 1.1 mmol). The resulting mixture was heated at reflux for 4 h using a Dean-Stark trap. The mixture was cooled to RT, concentrated by rotary evaporation and purified on silica gel (5:95 MeOH/CH2Cl2). The yellow solid obtained was dissolved in EtOAc (15 mL) and washed with a saturated solution of NH4Cl (aq). The organic phase was separated, dried over MgSO4, filtered and concentrated by rotary evaporation. The product was recrystallized from hexanes to afford the title compound as a white solid. EI-MS m/z 424 (M+H). Calc'd for C22H25N5O2S: 423.17.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06645990B2
Source datasetuspto-grants-2003_11
ORD IDord-859da533c9284a74a137695618de185e
Source noteuspto-grants-2003_11