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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1049741Generated: November 2, 2026

Acetonitrile → HCID 131736043, compound

https://huagongshe.com/reaction/1049741

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetonitrileHCID 6342—
ReactantAllyltributylstannaneHCID 90628—
ReactantHCID 71657160HCID 71657160—
SolventTolueneHCID 1140—
ProductHCID 131736043HCID 13173604368%

Reaction Conditions

Temperature110 °C

Reaction Steps

5-[4-(2-Iodobenzoylamino)phenyl]-1H-naphtho[1,2-b][1,4]diazepine-2,4(3H,5H)-dione (70 mg, 0.128 mmol), allyltributyltin (98 mg, 0.32 mmol), and tetrakistriphenylphosphine palladium(0) (15 mg, 12.8 μmol) were dissolved in anhydrous toluene (0.6 mL), and the solution was stirred at 110° C. for 16 hours. The reaction mixture was left to cool, and then added with acetonitrile, the mixture was washed with petroleum ether, and the solvent of the acetonitrile layer was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography (chloroform/methanol=100/1) to obtain the title compound (40 mg, yield 68%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382236B2
Source datasetuspto-grants-2016_07
ORD IDord-0c29225adc2e4596903ac1804c5716ce
Source noteuspto-grants-2016_07