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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1918769Generated: November 2, 2026

Dichloromethane → HCID 66832123, compound

https://huagongshe.com/reaction/1918769

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDichloromethaneHCID 6344—
ReactantIodobenzeneHCID 11575—
ReactantTriphenylphosphineHCID 11776—
ReactantHCID 66832046HCID 66832046—
CatalystBis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
CatalystHCID 178418647HCID 178418647—
SolventWaterHCID 962—
ProductHCID 66832123HCID 66832123—

Reaction Conditions

Temperature70 °C

Reaction Steps

Water (5 mL) was added to a pre-stirred mixture of N-(2-(5-chloro-1H-indol-3-yl)ethyl)oxazole-5-carboxamide intermediate 173 (0.107 g; 0.369 mmol), phenyl iodide (0.050 mL; 0.443 mmol), (1,1′-bis(diphenylphosphino)ferrocene)-dichloropalladium(II), complex with dichloromethane (0.015 g; 0.019 mmol), silver carbonate (0.204 g; 0.738 mmol) and triphenylphosphine (0.010 g; 0.037 mmol). The resulting mixture was stirred at 70° C. for 24 hours and after cooling down the mixture was partitioned between brine and dichloromethane. the two phases were separated and the aqueous layer was extracted with dichloromethane. The organic layer was dried and concentrated under reduced pressure. The crude mixture was purified by flash chromatography on silica (eluent 20 to 100% ethyl acetate in heptane) to yield 0.025 (19%) of the title compound as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08618138B2
Source datasetuspto-grants-2013_12
ORD IDord-6daf3ecfdc3c418a96139c4f0ea6013e
Source noteuspto-grants-2013_12