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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620140Generated: October 30, 2026

Potassium Carbonate → HCID 178491187, compound

https://huagongshe.com/reaction/1620140

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 178491183HCID 178491183—
Catalystpalladium(II) acetateHCID 167845—
Catalyst1,1`-Bis(diphenylphosphino)ferroceneHCID 15241612—
SolventDimethylformamideHCID 6228—
ProductHCID 178491187HCID 17849118787%

Reaction Conditions

Temperature100 °C

Reaction Steps

To a solution of [1-[{1-[4-(3-bromo-phenyl)-1H-imidazol-2-yl]-ethyl}-(3,4-dimethoxy-benzyl)-carbamoyl]-2-(4-carbamoyl-2,6-dimethyl-phenyl)-ethyl]-carbamic acid tert-butyl ester (290 mg; 0.40 mmol) in DMF (5 mL) was added K2CO3 (262 mg; 1.9 mmol) and the resulting mixture was degassed with Argon for 5 min. At this time, Pd(OAc)2 (8.9 mg; 0.04 mmol) and 1,1-bis(diphenylphosphino) ferrocene (46 mg; 0.083 mmol) were added. Carbon monoxide was then bubbled through the resulting mixture for 10 min at rt, the reaction was capped, and warmed to 100° C. for 6 h. After cooling to rt the mixture was partitioned between EtOAc and water, filtered through Celite, and then separated. The aqueous phase was then washed with a second portion of EtOAc. The aqueous phase was then acidified to pH 5 with 2N citric acid and the resulting aqueous solution extracted with EtOAc (4×). These latter EtOAc extracts were combined, dried over Na2SO4, filtered, and concentrated under reduced pressure to give the crude product (HPLC: 87% at 254 nm).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772325B2
Source datasetuspto-grants-2014_07
ORD IDord-89df05254f044da0b94fcd82d57f9d03
Source noteuspto-grants-2014_07