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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282306Generated: October 30, 2026

Acetic Acid → HCID 178419476, compound

https://huagongshe.com/reaction/2282306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantTolueneHCID 1140—
ReactantHydrazineHCID 9321—
ReactantDimethylformamide dimethyl acetalHCID 78373—
ReactantSodium BicarbonateHCID 516892—
Reactant2,4-Dibromothiazole-5-carboxamideHCID 58095249—
SolventEthyl acetate hexaneHCID 21226206—
ProductHCID 178419476HCID 17841947661.2%

Reaction Conditions

Temperature60 °C

Reaction Steps

To the suspension of 2,4-dibromo-1,3-thiazole-5-carboxamide (0.110 g, 0.385 mmol) in dry Toluene (8.0 mL, 75 mmol) was added DMFDMA (0.204 mL, 1.54 mmol). The mixture was stirred at 60° C. under N2 atmosphere for 3 hours. The solvent was removed and to the intermediate was added acetic acid (2.0 mL, 35 mmol), followed by hydrazine (0.0604 mL, 1.92 mmol). The mixture was heated to 120° C. for 30 min. The mixture was cooled to room temperature, solvent was removed and the residual acetic acid was azeotroped with toluene (2×5 mL) to give an oily material, which was basified with saturated aqueous NaHCO3 to pH˜8 and extracted with EtOAc (3×30 mL). The EtOAc layer was washed with water, brine, dried over Na2SO4, filtered, and evaporated to give a crude product. Chromatography on a silica column using EtOAc/hexane (0/100 to 50/50) gave a solid product (0.073 g, 61%). LCMS: (FA) ES+ 311 and ES− 309.111 NMR (400 MHz, d4-Methanol) 8.53 (s, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139589B2
Source datasetuspto-grants-2015_09
ORD IDord-808f767eb72c474c9432dafa2dd40551
Source noteuspto-grants-2015_09