HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1866845Generated: October 31, 2026
Potassium Carbonate → HCID 178491187, compound
https://huagongshe.com/reaction/1866845
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 178491183 | HCID 178491183 | — |
| Catalyst | palladium(II) acetate | HCID 167845 | — |
| Catalyst | 1,1`-Bis(diphenylphosphino)ferrocene | HCID 15241612 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 178491187 | HCID 178491187 | 87% |
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 room temperature, the reaction was capped, and warmed to 100° C. for 6 h. After cooling to room temperature 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 yield the crude product (HPLC: 87% at 254 nm).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07629488B2 |
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| Source dataset | uspto-grants-2009_12 |
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| ORD ID | ord-a90cb007768e446d8b60e3f5179b51cf |
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| Source note | uspto-grants-2009_12 |
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