HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 503837Generated: November 4, 2026
Potassium Carbonate → 4-Nitro-1-(pyridin-4-yl)methyl-1H-benzimidazole
https://huagongshe.com/reaction/503837
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Chloromethyl)pyridinium chloride | HCID 74570 | — |
| Reactant | 4-Nitrobenzimidazole | HCID 160949 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-Nitro-1-(pyridin-4-yl)methyl-1H-benzimidazole | HCID 59428631 | — |
Reaction Steps
A 500-mL round-bottomed flask equipped with a magnetic stirrer and nitrogen inlet is charged with compound 3b (3.30 g, 30.6 mmol), potassium carbonate (8.95 g, 64.8 mmol), anhydrous DMF (200 mL) and 4-chloromethylpyridine hydrochloride (3.98 g, 24.3 mmol) and the mixture is then stirred under nitrogen for 24 h at ambient temperature. After such time the reaction is partitioned between water (200 mL) and ethyl acetate (200 mL). The aqueous layer is separated and extracted with ethyl acetate (6×250 mL). The combined organic extracts are dried with sodium sulfate, and the drying agent is filtered off. The filtrate is then concentrated under vacuum to give a brown solid, which is purified by column chromatography to afford compound 3c as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07777040B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-c918527dc8004b3c900b8a787ee8dd87 |
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| Source note | uspto-grants-2010_08 |
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