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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1807688Generated: October 25, 2026

Ethyl Acetate → N-(8-methyl-4H-5-oxa-1-thia-3,7-diaza-cyclopenta[a]naphthalen-2-yl)-acetamide

https://huagongshe.com/reaction/1807688

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthyl AcetateHCID 8857—
ReactantCesium carbonateHCID 10796—
ReactantTributyl phosphine tetrafluoroborateHCID 71317416—
ReactantN-[4-(4-bromo-6-methyl-pyridin-3-yloxymethyl)-thiazol-2-yl]-acetamideHCID 86649535—
Catalystpalladium(II) acetateHCID 167845—
SolventDimethylformamideHCID 6228—
ProductN-(8-methyl-4H-5-oxa-1-thia-3,7-diaza-cyclopenta[a]naphthalen-2-yl)-acetamideHCID 8664953423.3%

Reaction Conditions

Temperature115 °C

Reaction Steps

A mixture of 463 mg (1.53 mmol) N-[4-(4-bromo-6-methyl-pyridin-3-yloxymethyl)-thiazol-2-yl]-acetamide (Stage 40.3), 900 mg (2.71 mmol) cesium carbonate, 30.4 mg (0.135 mmol) palladium acetate and 81 mg (0.271 mmol) tributylphosphine tetrafluoroborate in 3 mL DMF was stirred at 115° C. for 7 h under argon. Then the reaction mixture was poured onto water, EtOAc was added and, after filtration over a layer of Hyflo Super Gel medium (Fluka 56678), the filtrate was extracted with EtOAc (2×). The combined organic layers were washed with water and brine, dried (MgSO4) and filtered. The filtrate was concentrated in vacuo to leave a residue that was purified on silica gel (=−100% EtOAc in heptane) to afford 93 mg of the title compound as a solid. LCMS: tR=0.27 min, M+H=262, M−H 260 (method J).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08357707B2
Source datasetuspto-grants-2013_01
ORD IDord-43e8a293a40740648fd6caf581b35d73
Source noteuspto-grants-2013_01