HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 501444Generated: October 31, 2026
Dimethylformamide → t-Butyl 4-(3-benzyl-4-chloro-3H-imidazo(4,5-c]pyridin-2-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/501444
Participants
| Role | Name | HCID | Charge |
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| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | tert-Butyl piperazine-1-carboxylate | HCID 143452 | — |
| Reactant | 3-Benzyl-2,4-dichloro-1,3-dihydroimidazo[4,5-c]pyridine | HCID 57472844 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | t-Butyl 4-(3-benzyl-4-chloro-3H-imidazo(4,5-c]pyridin-2-yl)piperazine-1-carboxylate | HCID 23070589 | 14.9% |
Reaction Steps
0.094 g of t-butyl piperazine-1-carboxylate was added to a 1 ml N,N-dimethylformamide solution of 0.127 g of 3-benzyl-2,4-dichloro-1,3-dihydroimidazo[4,5-c]pyridine, and the mixture was heated at 150° C. for two hours. 25 ml of ethyl acetate was added to the mixture, and the organic layer was washed three times with 10 ml of water and then with 10 ml of an aqueous solution saturated with sodium chloride. The organic liquid was dried over magnesium sulfate, and concentrated under reduced pressure. The residue was purified by silica gel column chromatography. Thus, 0.029 g of the title compound was obtained from the fraction eluted with ethyl acetate-hexane (3:2).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07772226B2 |
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| Source dataset | uspto-grants-2010_08 |
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| ORD ID | ord-18f80efefcc84a9fb204b98854d12c0f |
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| Source note | uspto-grants-2010_08 |
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