HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 480821Generated: October 28, 2026
HCID 22393042, compound → HCID 10785324, compound
https://huagongshe.com/reaction/480821
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 22393042 | HCID 22393042 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 10785324 | HCID 10785324 | 83.5% |
Reaction Steps
A solution of 3-(Benzoxycarbonyl)amino-2,3-dihydro-1-(2-oxo-2-phenylethyl)-5-phenyl-1H-1,4-benzodiazepin-2-one (3.7 g, 7.36 mmol) in 100 mL of anhydrous methylene chloride was cooled to 0° C. under nitrogen. A stream of anhydrous HBr gas was then bubbled through this solution for 1 h. The bubbler was removed and the reaction was warmed to room temperature under nitrogen. After stirring 1 h the reaction was concentrated under vacuum and the residue was redissolved in 20 mL of methylene chloride. The crude HBr salt of the product was precipitated from solution using 300 mL of anhydrous ether and collected by filtration as a light yellow solid. After washing with ether , the solid was dissolved in methylene chloride and saturated sodium bicarbonate. The layers were separated and the organic layer was extracted with saturated sodium bicarbonate. The combined aqueous layers were then back extracted twice with methylene chloride. The combined organic layers were extracted once with water and dried over sodium sulfate. After concentration under vacuum, 2.27 g of the product was obtained as an orange foam which was carried on without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06653303B1 |
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| Source dataset | uspto-grants-2003_11 |
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| ORD ID | ord-1ae4657c8c124b6296ba0c5c8af36b4c |
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| Source note | uspto-grants-2003_11 |
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