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
Participants
| Role | Name | HCID | Charge |
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| Reactant | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Reactant | 1'-(5-iodo-1H-benzimidazol-2-yl)spiro[isobenzofuran-1,4'-piperidin]-3-one | HCID 178519032 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 178509526 | HCID 178509526 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06566367B2 |
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| Source dataset | uspto-grants-2003_05 |
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| ORD ID | ord-4c17649609a4440488c2c7c52dd112cd |
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| Source note | uspto-grants-2003_05 |
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