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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2173278Generated: October 31, 2026

Nitrogen → HCID 67518235, compound

https://huagongshe.com/reaction/2173278

Reaction equation

Participants

RoleNameHCIDCharge
ReactantNitrogenHCID 947—
ReactantDimethylformamideHCID 6228—
ReactantHCID 67515563HCID 67515563—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
CatalystHCID 178418397HCID 178418397—
SolventEthyl AcetateHCID 8857—
ProductHCID 67518235HCID 67518235—

Reaction Steps

A solution of tert-butyl 4-[(6-fluoro-5-iodo-3,4-dihydro-1H-isochromen-1-yl)methyl]piperazine-1-carboxylate (200 mg, 0.42 mmol), Pd(PPh3)4 (200 mg) and Zn(CN)2 (300 mg, 2.6 mmol) in 20 mL of anhydrous DMF was to 110° C. at N2 atmosphere for 2 hours. The reaction was cooled to room temperature, diluted with EtOAc and washed with water and brine. The organic layer was dried over anhydrous sodium sulfate and concentrated. The residue was purified with prep-TLC to afford tert-butyl 4-[(5-cyano-6-fluoro-3,4-dihydro-1H-isochromen-1-yl)methyl]piperazine-1-carboxylate.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09056859B2
Source datasetuspto-grants-2015_06
ORD IDord-15cf1812d60041db8b0ee31179edb85a
Source noteuspto-grants-2015_06