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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1625001Generated: November 4, 2026

1,4-Dioxane → HCID 24804886, compound

https://huagongshe.com/reaction/1625001

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
Reactant1,8-Diazabicyclo(5.4.0)undec-7-eneHCID 81184—
ReactantBenzenemethanamine, 4-chloro-3-(trifluoromethyl)-HCID 485440—
ReactantHCID 67203856HCID 67203856—
CatalystMolybdenum carbonyl (Mo(CO)6)HCID 98885—
Catalystpalladium(II) acetateHCID 167845—
ProductHCID 24804886HCID 24804886—

Reaction Conditions

Temperature110 °C

Reaction Steps

A 5-mL process vial was charged with (S)-2-(5-iodo-1-oxoisoquinolin-2(1H)-yl)propanamide (100 mg, 0.0004 mol), (4-chloro-3-(trifluoromethyl)phenyl)methanamine (200 mg, 0.001 mol), molybdenum hexacarbonyl (90 mg, 0.0004 mol), palladium acetate (8 mg, 0.00004 mol), 1,8-diazabicyclo[5.4.0]undec-7-ene (200 mg, 0.001 mol) and 1,4-dioxane (2 mL, 0.02 mol). The vessel was sealed under air and exposed to microwave heating for 15 min at 110° C. The reaction tube was thereafter cooled to room temperature, and the mixture was concentrated and dissolved in a small volume of dichloromethane. The crude product was purified via flash column chromatography (12 g of silica gel, 50-100% EtOAC/Hexane) to give the desired product as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08779144B2
Source datasetuspto-grants-2014_07
ORD IDord-7bf0be70dc2244e9bade659bc6ddd09f
Source noteuspto-grants-2014_07