HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1173949Generated: October 27, 2026
Triethylamine → 4-{[bis(1-heptyloxycarbonyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-N-(4-dipropylaminomethylphenyl)-benzamide
https://huagongshe.com/reaction/1173949
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Carbonochloridic acid, heptyl ester | HCID 118547 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-{[bis(1H-imidazol-2-ylmethyl)-amino]-methyl}-N-(4-dipropylaminomethylphenyl)-benzamide | HCID 9983420 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-{[bis(1-heptyloxycarbonyl-1H-imidazol-2-ylmethyl)-amino]-methyl}-N-(4-dipropylaminomethylphenyl)-benzamide | HCID 58801920 | — |
Reaction Steps
The compound (83.8 mg) obtained in Example 19-3 was dissolved in anhydrous dichloromethane (1.5 ml). The solution was added with triethylamine (70.1 μl) and then added with n-heptyl chloroformate (74.9 μl) in an ice bath, followed by stirring overnight under a nitrogen atmosphere at room temperature. After completion of the reaction, the solution was added with a saturated aqueous sodium bicarbonate solution and stirred for a while. Then, the solution was extracted with chloroform and washed with a saturated aqueous sodium bicarbonate solution and saturated saline solution. The organic layer was dried with anhydrous sodium sulfate. Subsequently, the solvent was distilled off and the residue was then purified through silica gel column chromatography (chloroform/methanol), thereby obtaining the subject compound (111 mg) as a brown solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07833991B2 |
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| Source dataset | uspto-grants-2010_11 |
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| ORD ID | ord-a8f549617e6440d4a338f3c3a8c476f9 |
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| Source note | uspto-grants-2010_11 |
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