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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2093679Generated: October 25, 2026

Acetic Acid → 2-(1H-pyrazol-3-yl)-1,3-thiazole

https://huagongshe.com/reaction/2093679

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantHydrazineHCID 9321—
Reactant2-AcetylthiazoleHCID 520108—
ReactantN,N-dimethylformamide N,N-dimethylacetamideHCID 22628260—
SolventDichloromethaneHCID 6344—
Product2-(1H-pyrazol-3-yl)-1,3-thiazoleHCID 3363559100%

Reaction Steps

Dissolved 1-(thiazol-2-yl)ethanone (1-BA-1, 5 g, 39.7 mmole) in DMF DMA (9.5 g, 2 eq). The resulting mixture was warmed to 100° C. until all the ketone starting material was consumed. This material was concentrated under reduced pressure to give 6.5 g of crude intermediate. This material was dissolved in 25 mL of DCM and 5 mL of HOAc was added, followed by hydrazine (5 g, 4 eq) at 0° C. The resulting mixture was heated at reflux until all the starting material was consumed. The reaction mixture was cooled to rt and neutralized with 30 mL of a saturated NaHCO3 solution. The layers were separated and the aqueous layer was extracted with DCM (2×50 mL). The organic layers were dried over MgSO4, filtered, and concentrated under reduced pressure. The crude material was purified by MPLC (eluted with 0-20% MeOH/DCM) to give 2-(1H-pyrazol-5-yl)thiazole (Compound 2-BA-1, ˜6 g). LC/MS: 152.0 m/z (M+H)+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08445503B2
Source datasetuspto-grants-2013_05
ORD IDord-edb57215d5a14a1fa828bb86aaf09c38
Source noteuspto-grants-2013_05