HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 348670Generated: October 30, 2026
1H-imidazole-2-carbaldehyde → (4-dipropylaminobutyl)-(4-{[(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)carbamic Acid t-butyl Ester
https://huagongshe.com/reaction/348670
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1H-imidazole-2-carbaldehyde | HCID 24955 | — |
| Reactant | (4-aminomethylbenzyl)-(4-dipropylaminobutyl)carbamic Acid t-butyl Ester | HCID 66941409 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (4-dipropylaminobutyl)-(4-{[(1H-imidazol-2-ylmethyl)amino]methyl}benzyl)carbamic Acid t-butyl Ester | HCID 66941456 | 107.5% |
Reaction Steps
The compound (0.78 g) obtained in Example 25-4 was dissolved in methanol (20 ml) and added with 2-imidazole carboxaldehyde (214.6 mg), followed by stirring at room temperature for 17 hours. After the solvent had been distilled off, the residue was dried under vacuum and then dissolved in methanol (15 ml) and then added with sodium borohydride (217.8 mg), followed by stirring at room temperature for 45 minutes. The reaction solution was added with a saturated aqueous ammonium chloride solution (10 ml) and stirred at room temperature for 15 minutes. Then, the reaction solution was added with saturated saline solution and extracted with chloroform, followed by drying with anhydrous sodium sulfate. After the solvent had been distilled off, the residue obtained was purified through silica gel column chromatography (chloroform/ethyl acetate), thereby obtaining the subject compound (1.01 g) as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07176227B2 |
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| Source dataset | uspto-grants-2007_02 |
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| ORD ID | ord-ed6ecaad2332453286c9b2c01a3f55f3 |
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| Source note | uspto-grants-2007_02 |
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