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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 413238Generated: October 29, 2026

N-methyl-2-pyrrolidone → HCID 178509526, compound

https://huagongshe.com/reaction/413238

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant1'-(5-iodo-1H-benzimidazol-2-yl)spiro[isobenzofuran-1,4'-piperidin]-3-oneHCID 178519032—
CatalystZinc cyanide (Zn(CN)2)HCID 11186—
SolventEthyl AcetateHCID 8857—
ProductHCID 178509526HCID 178509526—

Reaction Conditions

Temperature130 °C

Reaction Steps

Add zinc cyanide (0.016 g, 0.13 mmol) and tetrakistriphenylphosphine palladium(0) (0.018 g, 0.02 mmol) to a solution of 1′-(5-iodo-1H-benzimidazol-2-yl)-spiro[isobenzofuran-1,4′-piperidin]-3-one (0.1 g, 0.22 mmol) in NMP (2 mL). Heat the reaction mixture at 130° C. for 19 hours. After cooling to ambient temperature, dilute the mixture with EtOAc (20 mL), and wash with water (20 mL) and saturated aqueous NaCl (20 mL). Dry the organic portion over Na2SO4, filter and concentrate. Purify by preparative TLC (80% EtOAc-hexane) to obtain 1′-(5-cyano-1H-benzimidazol-2-yl)-spiro[isobenzofuran-1,4′-piperidin]-3-one as a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06566367B2
Source datasetuspto-grants-2003_05
ORD IDord-4c17649609a4440488c2c7c52dd112cd
Source noteuspto-grants-2003_05