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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 390713Generated: October 23, 2026

Cesium carbonate → HCID 178429941, compound

https://huagongshe.com/en/reaction/390713

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
Reactant1,3-Dichloro-5-iodobenzeneHCID 76424—
Reactant5-Chloro-1,10-phenanthrolineHCID 77865—
Reactant2,2-dimethyl-N-(5-methyl-1,3-thiazol-2-yl)propanamideHCID 17190929—
ReactantWater ammonium hydroxideHCID 86589665—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 178429941HCID 178429941—

Reaction Conditions

Temperature120 °C

Reaction Steps

In a 4 mL vial charged with a stir bar, 2,2-dimethyl-N-(5-methyl-1,3-thiazol-2-yl)propanamide (71 mg, 0.35 mmol) was added, followed by copper(I) trifluoromethanesulfonate benzene complex (35 mg, 0.07 mmol), 5-chloro-1,10-phenanthroline (30 mg, 0.14 mmol) and cesium carbonate (126 mg, 0.39 mmol). A loose cap with septum was placed on the vial and the vial was placed under vacuum in a vacuum oven for 30 minutes. The solid mixture was purged with nitrogen gas a couple of times. Then 1,3-dichloro-5-iodobenzene (115 mg, 0.42 mmol) dissolved in 1-methyl-2-pyrrolidinone (1.0 mL) was added to the solid mixture. The vial was capped and placed on a heater/stirrer and heated to 120° C. overnight. Then a 1 mL solution of concentrated ammonium hydroxide/water (1:2) was added. The reaction was filtered and concentrated to dryness. The residue was purified by reverse phase HPLC (C8, gradient 10-100% acetonitrile/water/0.1% trifluoroacetic acid).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08383657B2
Source datasetuspto-grants-2013_02
ORD IDord-247e4401033944dd8c4df11346919a95
Source noteuspto-grants-2013_02