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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1627232Generated: October 31, 2026

Sodium Carbonate → HCID 136340996, compound

https://huagongshe.com/reaction/1627232

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
ReactantHCID 58506151HCID 58506151—
ReactantHCID 66989360HCID 66989360—
SolventTolueneHCID 1140—
SolventEthyl AcetateHCID 8857—
ProductHCID 136340996HCID 136340996—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 4,5-dibromo-1-(2-trimethylsilanyl-ethoxymethyl)-1H-imidazole-2-carboxylic acid(pyridin-4-ylmethyl)-amide (280 mg, 0.57 mmol) and 2-(3-methyl-1,2,4-oxadiazol-5-yl)-5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-indole-1-carboxylic acid tert-butyl ester (243 mg, 0.57 mmol) in toluene (5.0 ml) is added aqueous Na2CO3 solution (2M, 0.63 ml, 1.26 mmol). The mixture is purged with argon for 10 minutes. (Bis(di-t-butyl(4-dimethylaminutesophenyephosphine)dichloropalladium(II) (81 mg, 0.11 mmol) is added and the reaction mixture is sealed in a sealed tube and heated to 120° C. for 14 hours. The reaction mixture is diluted with ethyl acetate (25 ml), washed with water (15 ml), brine (15 ml), dried over MgSO4, filtered, and concentrated in vacuo. The crude material is purified on reversed phase HPLC. The resulting protected analog is dissolved in 50% trifluoroacetic acid in dichloromethane (10 ml). After 2 hours the solvent is evaporated in vacuo, and the product is purified by reverse phase HPLC, 25 mg, 9%, LC/MS ESI m/z (M+H)+=480.33.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08785489B2
Source datasetuspto-grants-2014_07
ORD IDord-352639ac86954d269f6e8f84f9775829
Source noteuspto-grants-2014_07