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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2364049Generated: October 29, 2026

Acetone → 6-(5-ethyl-1H-pyrazol-4-yl)-1,2,2-trimethyl-2,3-dihydrothieno[3,2-d]pyrimidin-4(1H)-one

https://huagongshe.com/reaction/2364049

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
Reactantp-Toluenesulfonic acidHCID 6101—
ReactantTrifluoroacetic acidHCID 6422—
ReactantSulfuric acid magnesium salt (1:1)HCID 24083—
ReactantSodium BicarbonateHCID 516892—
Reactant5-ethyl-N,N-dimethyl-4-(1,2,2-trimethyl-4-oxo-1,2,3,4-tetrahydrothieno[3,2-d]pyrimidin-6-yl)-1H-pyrazole-1-sulfonamideHCID 66743610—
SolventDimethylformamideHCID 6228—
Product6-(5-ethyl-1H-pyrazol-4-yl)-1,2,2-trimethyl-2,3-dihydrothieno[3,2-d]pyrimidin-4(1H)-oneHCID 6674387744%

Reaction Steps

A mixture of 5-ethyl-N,N-dimethyl-4-(1,2,2-trimethyl-4-oxo-1,2,3,4-tetrahydrothieno[3,2-d]pyrimidin-6-yl)-1H-pyrazole-1-sulfonamide (129 mg, 0.325 mmol) and TFA (2.00 mL, 26.0 mmol) was stirred for 1 h at room temperature. The mixture was poured into saturated aqueous NaHCO3 and extracted with EtOAc, and the extract was dried over MgSO4, filtered and concentrated under reduced pressure. The residue was mixed with acetone (5 mL, 68.1 mmol), MgSO4 (78 mg, 0.649 mmol), PTSA (6.2 mg, 0.032 mmol) and DMF (1 mL). This mixture was stirred at 60° C. for 1 h. The mixture was poured into saturated aqueous NaHCO3 and extracted with 3:1 EtOAc/THF, and the extract was dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by column chromatography (Purif, silica gel, hexane to EtOAc then to 80:20 EtOAc/MeOH). The obtained solid was triturated with EtOAc and collected by filtration to afford the title compound (41.2 mg, 44%) as a pale yellow solid:

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08691828B2
Source datasetuspto-grants-2014_04
ORD IDord-6c08ca758d4344a79aa297727e9070aa
Source noteuspto-grants-2014_04