HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 893663Generated: October 30, 2026
Potassium Iodide → HCID 13587988, compound
https://huagongshe.com/reaction/893663
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Picolyl chloride hydrochloride | HCID 23392 | — |
| Reactant | 1-Piperidinecarboxylic acid, 4-(1H-benzimidazol-2-ylamino)-, ethyl ester | HCID 3018455 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13587988 | HCID 13587988 | 40% |
Reaction Steps
A mixture of 57.5 parts of ethyl 4-(1H-benzimidazol-2-ylamino)-1-piperidinecarboxylate, 33 parts of 2-(chloromethyl)pyridine hydrochloride, 43 parts of sodium carbonate, 0.1 parts of potassium iodide and 630 parts of N,N-dimethylformamide was stirred and heated overnight at 70° C. The reaction mixture was cooled and poured onto water. The product was extracted with 4-methyl-2-pentanone. The extract was dried, filtered and evaporated. The residue was purified by column chromatography over silica gel using a mixture of trichloromethane and methanol (96:4 by volume) as eluent. The pure fractions were collected and the eluent was evaporated. The residue was crystallized form 4-methyl-2-pentanone, yielding 30 parts (40%) of ethyl 4-[[1-[(2-pyridinyl)methyl]-1H-benzimidazol-2-yl]amino]-1-piperidinecarboxylate; mp. 161.5° C. (intermediate 60).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05126339 |
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| Source dataset | uspto-grants-1992_06 |
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| ORD ID | ord-377bfd9d83124b6284e7d5d2ee39ec2d |
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| Source note | uspto-grants-1992_06 |
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