Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775354Generated: November 3, 2026

Diisopropylethylamine → Ethyl 2-(4-tert-butoxycarbonylpiperazin-1-yl)-5-methylamino-thiazole-4-carboxylate

https://huagongshe.com/reaction/1775354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactanttert-Butyl piperazine-1-carboxylateHCID 143452—
ReactantEthyl 2-bromo-5-(methylamino)-1,3-thiazole-4-carboxylateHCID 53613688—
Solvent1,4-DioxaneHCID 31275—
ProductEthyl 2-(4-tert-butoxycarbonylpiperazin-1-yl)-5-methylamino-thiazole-4-carboxylateHCID 8982582835.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of ethyl 2-bromo-5-methylamino-thiazole-4-carboxylate (401 mg, 1.512 mmol) and tert-butyl piperazine-1-carboxylate (1.06 g, 5.69 mmol) in anhydrous dioxane (15 ml) was added DIPEA (2 ml, 11.5 mmol) and the reaction was heated at 100° C. in a sealed flask for 23 hours. The mixture was cooled to room temperature, partitioned between DCM and sat. sodium bicarbonate solution and the phases were separated. The aqueous layer was extracted twice with DCM and the combined organic layers were dried (sodium sulfate) and concentrated under reduced pressure. The residue was purified by column chromatography (silica, gradient from 10 to 70% ethyl acetate in n-heptane) to yield 197 mg of a white solid (0.532 mmol, yield 35%) MS (multi-mode) m/z=371.2 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-17f9f95bb6a346e9a3b2526fc373f2b1
Source noteuspto-grants-2016_02