HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333442Generated: October 30, 2026
Hydrochloric Acid → (1H-imidazol-4-yl)methanamine dihydrochloride
https://huagongshe.com/reaction/333442
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethanol | HCID 702 | — |
| Reactant | Tetrahydrofuran | HCID 8028 | — |
| Reactant | Piperidin-1-yl-(1-trityl-1H-imidazol-4-yl-methylene)amine | HCID 66987946 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | (1H-imidazol-4-yl)methanamine dihydrochloride | HCID 178478688 | 29% |
Reaction Steps
To a solution containing 450 mg of piperidin-1-yl-(1-trityl-1H-imidazol-4-yl-methylene)amine in 3.5 mL of 3N hydrogen chloride in ethyl acetate are added 90 mg of 10% Pd/C, 0.5 mL of THF and 0.9 mL of ethanol. The reaction medium is placed under a hydrogen pressure of 6 bar and heated at 80° C. for 3 hours. After filtering off the catalyst and evaporating off the solvents, the crude product obtained is chromatographed on silica gel (eluent: 6/4 DCM/MeOH). 50 mg of C-(1H-imidazol-4-yl)methylamine dihydrochloride in the form of a white powder are obtained in a yield of 29%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08877968B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-32f171c68d024b799c116604e161a63e |
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| Source note | uspto-grants-2014_11 |
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