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WO2002005747A3 - The process of manufacturing pharmaceutical grade tannates - Google Patents

The process of manufacturing pharmaceutical grade tannates Download PDF

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Publication number
WO2002005747A3
WO2002005747A3 PCT/IB2001/001254 IB0101254W WO0205747A3 WO 2002005747 A3 WO2002005747 A3 WO 2002005747A3 IB 0101254 W IB0101254 W IB 0101254W WO 0205747 A3 WO0205747 A3 WO 0205747A3
Authority
WO
WIPO (PCT)
Prior art keywords
tannates
tannic acid
isopropanol
tannate
antihistamine
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Ceased
Application number
PCT/IB2001/001254
Other languages
French (fr)
Other versions
WO2002005747A2 (en
Inventor
Chidambaram Venkate Srinivasan
Mamilla Srinivas Reddy
Bakulesh Mafatlal Khamar
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Cadila Pharmaceuticals Ltd
Original Assignee
Cadila Pharmaceuticals Ltd
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Cadila Pharmaceuticals Ltd filed Critical Cadila Pharmaceuticals Ltd
Publication of WO2002005747A2 publication Critical patent/WO2002005747A2/en
Publication of WO2002005747A3 publication Critical patent/WO2002005747A3/en
Anticipated expiration legal-status Critical
Ceased legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K47/00Medicinal preparations characterised by the non-active ingredients used, e.g. carriers or inert additives; Targeting or modifying agents chemically bound to the active ingredient
    • A61K47/06Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite
    • A61K47/08Organic compounds, e.g. natural or synthetic hydrocarbons, polyolefins, mineral oil, petrolatum or ozokerite containing oxygen, e.g. ethers, acetals, ketones, quinones, aldehydes, peroxides
    • A61K47/10Alcohols; Phenols; Salts thereof, e.g. glycerol; Polyethylene glycols [PEG]; Poloxamers; PEG/POE alkyl ethers

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • General Chemical & Material Sciences (AREA)
  • Oil, Petroleum & Natural Gas (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Antihistamines are available in the form of fee bases as well as salt i.e. hydrochloride, maleate, tannate, etc. Frequently, it is necessary to utilise antihistamines in the form of tannate salt because such salts are generally quite stable and may be administered in such from without untoward side effects. Tannic acid, also known as tannin, is a well know naturally occurring substance. Tannic acid, which is available commercially, usually contain about 5 % of water, has a molecular weight of about 1700 and is typically produced from Turkish or Chinese nutgall. Antihistamine tannates, presently manufactured commercially, are relatively impure. Such tannates are prepared by the reaction of antihistamine free base with tannic acid and using a volatile solvent, isopropanol (IPA). The yield is only fair (around 70 %) and decomposition products e.g. 2-5 % along with significant amount of volatile solvent, isopropanol (6-10 %) remains with the product, which cannot be removed. According to present invention, the tannates are made by dissolving tannic acid and amine in different compatible solvents. The solvents can be halogenated alkanes or alkanoic esters. The examples of halogenated alkane is chloroform, and that of alkanoic ester is ethyl acetate. This avoids the use of isopropanol. This method gives tannates which are lighter in colour. Ephedrine and Pseudoephredine tannates are prepared by using ethyl acetate as a medium for reactions to get pharmaceutical grade tannate.
PCT/IB2001/001254 2000-07-14 2001-07-13 The process of manufacturing pharmaceutical grade tannates Ceased WO2002005747A2 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
IN661/MUM/2000 2000-07-14
IN661MU2000 2000-07-14

Publications (2)

Publication Number Publication Date
WO2002005747A2 WO2002005747A2 (en) 2002-01-24
WO2002005747A3 true WO2002005747A3 (en) 2002-10-10

Family

ID=11097264

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/IB2001/001254 Ceased WO2002005747A2 (en) 2000-07-14 2001-07-13 The process of manufacturing pharmaceutical grade tannates

Country Status (1)

Country Link
WO (1) WO2002005747A2 (en)

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
PL364087A1 (en) 2001-02-21 2004-12-13 Basf Aktiengesellschaft Method for the production of d-pantothenic acid and/or salts thereof as adjunct for animal feedstuffs
US20030114535A1 (en) 2001-12-14 2003-06-19 Jame Fine Chemicals, Inc. Dextrochlorpheniramine tannate
US6677381B1 (en) 2001-12-14 2004-01-13 Jame Fine Chemicals, Inc. Guaifenesin tannate
US6670370B1 (en) 2001-12-14 2003-12-30 Jame Fine Chemicals, Inc. Dextromethorphan tannate

Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3282789A (en) * 1963-05-17 1966-11-01 Neisler Lab Inc Stable liquid colloidal tannate compositions
US5599846A (en) * 1996-06-28 1997-02-04 Jame Fine Chemicals, Inc. Phenylephrine tannate compositions
US5663415A (en) * 1996-06-28 1997-09-02 Jame Fine Chemicals, Inc. Process for preparing antihistamine tannates

Patent Citations (3)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3282789A (en) * 1963-05-17 1966-11-01 Neisler Lab Inc Stable liquid colloidal tannate compositions
US5599846A (en) * 1996-06-28 1997-02-04 Jame Fine Chemicals, Inc. Phenylephrine tannate compositions
US5663415A (en) * 1996-06-28 1997-09-02 Jame Fine Chemicals, Inc. Process for preparing antihistamine tannates

Also Published As

Publication number Publication date
WO2002005747A2 (en) 2002-01-24

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