HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 848550Generated: October 30, 2026
Hydrogen Bromide → HCID 20562331, compound
https://huagongshe.com/reaction/848550
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Hydrogen Bromide | HCID 260 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 20562388 | HCID 20562388 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 20562331 | HCID 20562331 | — |
Reaction Steps
200 mg (0.4 mM) of 1-benzyl-1-(2-tert.butoxyethyl)-3-[5-(o-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7-yl]urea are heated on a steam-bath for 10 minutes in 3 ml of a 33% solution of hydrogen bromide in glacial acetic acid and then left to stand at room temperature for 3 days. The mixture is neutralised with sodium bicarbonate and extracted several times with methylene chloride. The methylene chloride extracts are combined, dried over sodium sulphate, filtered and concentrated. The residue is purified in a pressure column (0.2-0.4 atmospheres of nitrogen) on 15 g of silica gel (particle size 0.04-0.06 mm) using ethyl acetate as the eluting agent and crystallised from ethyl acetate/ether, there being obtained 2-[3-[5-(o-fluorophenyl)-2,3-dihydro-1-methyl-2-oxo-1H-1,4-benzodiazepin-7yl]ureido]ethyl acetate which melts at 196°-198° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04296031 |
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| Source dataset | uspto-grants-1981_10 |
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| ORD ID | ord-8b5a6851b48c40e9a5bb953098dfd461 |
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| Source note | uspto-grants-1981_10 |
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