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US Patent 6350870 - Process for preparing pure crystalline lorazepam

US Patent Issued on February 26, 2002
Estimated Patent Expiration Date: Icon_subject March 5, 2021Estimated Expiration Date is calculated based on simple USPTO term provisions. It does not account for terminal disclaimers, term adjustments, failure to pay maintenance fees, or other factors which might affect the term of a patent.
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Abstract

The present invention provides a process for preparing crystalline lorazepam substantially free of bound solvent from a lorazepam alcohol solvate or hydrate by suspending the lorazepam solvate in an organic medium selected from ethyl acetate, cyclohexane, dichloromethane, toluene and mixtures thereof. This process is useful in producing the anti-anxiety and sedative agent lorazepam in increased yields. A process for converting lorazepam lower alcohol solvates to lorazepam hydrate is also disclosed.

Inventor

Assignee

Application

No. 799318 filed on 03/05/2001

US Classes:

540/507The additional chalcogen is bonded directly at the 3-position of the bicyclo ring system

Field of Search

540/507The additional chalcogen is bonded directly at the 3-position of the bicyclo ring system

Examiners

Primary: Kifle, Bruck

Attorney, Agent or Firm

US Patent References

3296249

International Classes

C07D 243/24
C07D 243/26

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