HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2417492Generated: November 3, 2026
Acetic Acid → 1-[4-(2,5-Dihydro-1h-pyrrol-1-ylcarbonyl)benzyl]-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on hydrochloride
https://huagongshe.com/reaction/2417492
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Di-tert-butyl dicarbonate | HCID 90495 | — |
| Reactant | Sodium triacetoxyborohydride | HCID 5049666 | — |
| Reactant | Ethyl (2-nitrobenzyl)aminoacetate | HCID 13236074 | — |
| Reactant | 4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benz-aldehyde | HCID 22632597 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 1-[4-(2,5-Dihydro-1h-pyrrol-1-ylcarbonyl)benzyl]-1,3,4,5-tetrahydrobenzo[e][1,4]diazepin-2-on hydrochloride | HCID 22632355 | — |
Reaction Steps
2.0 g (8.47 mmol) of ethyl (2-nitrobenzyl)aminoacetate was dissolved in 20 ml of dichloromethane. 2.7 g (12.6 mmol) of di-t-butyl dicarbonate and 2.4 ml (16.9 mmol) of triethylamine were added to the obtained solution, and they were stirred at room temperature overnight. After the treatment with dichloromethane as the extracting solvent by an ordinary method, 200 mg of 10% palladium/carbon was added to the obtained crude product and they were stirred in the presence of hydrogen at room temperature for 5 hours. The reaction solution was filtered through Celite. The solvent was evaporated and the obtained crude product was dissolved in 20 ml of dichloromethane. 670 mg (3.29 mmol) of 4-(2,5-dihydro-1H-pyrrol-1-ylcarbonyl)benzaldehyde and 0.29 ml (5.1 mmol) of acetic acid were added to the obtained solution, and they were stirred at room temperature for 30 minutes. 1.3 g (6.3 mmol) of sodium triacetoxyborohydride was added to the reaction mixture, and they were stirred at room temperature overnight. After the treatment with dichloromethane as the extracting solvent by an ordinary method, the obtained crude product was dissolved in a mixture of 2 ml of 1 N sodium hydroxide and 4 ml of ethanol, and the obtained solution was stirred at room temperature for 5 hours. After the treatment with ethyl acetate as the extracting solvent by an ordinary method, the obtained crude product was dissolved in 10 ml of dichloromethane. 78 mg (3.29 mmol) of 2-chloro-1,3-dimethylimidazonium chloride and 0.71 ml (5.1 mmol) of triethylamine were added to the obtained solution, and they were stirred overnight. After the treatment with dichloromethane as the extracting solvent by an ordinary method, the obtained crude product was dissolved in 5 ml of 4N solution of hydrogen chloride in dioxane, and the obtained solution was stirred at room temperature for 3 hours. The solvent was evaporated to obtain the crude title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06825191B2 |
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| Source dataset | uspto-grants-2004_11 |
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| ORD ID | ord-c55f9246d6e344898ae2d33ab16a7779 |
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| Source note | uspto-grants-2004_11 |
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