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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 563992Generated: October 26, 2026

Ethyl 5-hydrazinyl-1,3-thiazole-4-carboxylate → ethyl 5-[4-(2-methoxy-2-oxoethyl)-3-methyl-5-(pyridin-2-yl)-1H-pyrazol-1-yl]-1,3-thiazole-4-carboxylate

https://huagongshe.com/reaction/563992

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl 5-hydrazinyl-1,3-thiazole-4-carboxylateHCID 55281999—
ReactantMethyl 4-oxo-3-(pyridin-2-ylcarbonyl)pentanoateHCID 67005342—
SolventMethanolHCID 887—
Productethyl 5-[4-(2-methoxy-2-oxoethyl)-3-methyl-5-(pyridin-2-yl)-1H-pyrazol-1-yl]-1,3-thiazole-4-carboxylateHCID 6700551668.8%

Reaction Conditions

Temperature90 °C

Reaction Steps

In a microwave reactor, 0.358 g (1.91 mmol) of ethyl 5-hydrazinyl-1,3-thiazole-4-carboxylate were added to 0.450 g (1.91 mmol) of methyl 4-oxo-3-(pyridin-2-ylcarbonyl)pentanoate in 4 ml methanol. In a microwave oven the closed vessel was heated at 90° C. for 2 hours. After removal of the solvent, the residue was extracted repeatedly with dichloromethane/water. The combined organic phases were dried over sodium sulfate and the solvent was removed under reduced pressure. Chromatography of the residue gave 0.508 g of product (61.8% of theory), NMR (CDCl3, 300 MHz): 1.12 (t, 3H); 2.35 (s, 3H); 3.66 (s, 2H); 3.69 (s, 3H); 4.08 (s, 3H); 7.19 (m, 1H); 7.32 (m, 1H); 7.66 (m, 1H); 8.51 (m, 1H); 8.72 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08067611B2
Source datasetuspto-grants-2011_11
ORD IDord-72cf2f2bd8eb4815ae1b0cbd16ced40c
Source noteuspto-grants-2011_11