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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2282334Generated: November 1, 2026

Acetic Acid → HCID 58094826, compound

https://huagongshe.com/reaction/2282334

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantPhenylsilaneHCID 12752—
ReactantSodium BicarbonateHCID 516892—
ReactantHCID 58095014HCID 58095014—
CatalystHCID 178418397HCID 178418397—
SolventDichloromethaneHCID 6344—
ProductHCID 58094826HCID 5809482659%

Reaction Conditions

Temperature40 °C

Reaction Steps

A mixture of 7-[5-(1-allyl-1H-imidazol-2-yl)-4-(2,4-dichlorophenyl)-2-thienyl][1,3]thiazolo[5,4-d]pyrimidin-2-amine (28.0 mg, 0.058 mmol), acetic acid (2.0 mL) and DCM (6.0 mL) was degassed with vacuum and then the atmosphere was replaced with nitrogen. To the mixture, were added tetrakis(triphenylphosphine)palladium(0) (7.03 mg, 0.00608 mmol) and phenylsilane (0.10 mL, 0.81 mmol). The resulting mixture was stirred at 40° C. for 30 min. The mixture was allowed to cool to rt followed by adding sat. NaHCO3 and DCM. After being stirred for 10 min, the organic layer was washed with brine, dried over anhydrous sodium sulfate, filtered and concentrated in vacuo. Column chromatography was performed to yield the title compound (15.1 mg, 59%) as a pale yellow solid. LCMS: (AA) ES+445, 447. 1H NMR (400 MHz, d6-DMSO) δ: 11.82 (bs, 1H), 8.64 (s, 1H), 8.39-8.37 (m, 2H), 7.73 (d, J=2.0 Hz, 1H), 7.64-7.42 (m, 3H), 7.12 (bs, 1H), 6.95 (bs, 1H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09139589B2
Source datasetuspto-grants-2015_09
ORD IDord-f4bb6bd53f8e4b18af526b5cdff512b5
Source noteuspto-grants-2015_09