GB1469384A - Tetracyclines - Google Patents

Tetracyclines

Info

Publication number
GB1469384A
GB1469384A GB2627075A GB2627075A GB1469384A GB 1469384 A GB1469384 A GB 1469384A GB 2627075 A GB2627075 A GB 2627075A GB 2627075 A GB2627075 A GB 2627075A GB 1469384 A GB1469384 A GB 1469384A
Authority
GB
United Kingdom
Prior art keywords
hydrogen atom
group
carbon atoms
represented
methylthioalkyl
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.)
Expired
Application number
GB2627075A
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.)
Pfizer Italia SRL
Original Assignee
Farmaceutici Italia SpA
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 Farmaceutici Italia SpA filed Critical Farmaceutici Italia SpA
Publication of GB1469384A publication Critical patent/GB1469384A/en
Expired legal-status Critical Current

Links

Abstract

1469384 Alkyl- and methylthioalkyl-tetracyclines SOC FARMACEUTICI ITALIA SpA 20 June 1975 [25 June 1974] 26270/75 Heading C2C A tetracycline of the general Formula I wherein R 1 represents a hydrogen atom, a hydroxy group or an acyloxy group having from 1 to 4 carbon atoms; R 2 represents a hydrogen atom or a methyl group; R 3 represents a hydrogen atom when R 2 represents a methyl group or otherwise represents a hydrogen atom, an alkyl group having from 1 to 4 carbon atoms, a methylthioalkyl group having from 2 to 5 carbon atoms or a dimethylamino group; R 4 represents a hydrogen atom when R 3 represents a dimethylamino group or otherwise represents a hydrogen atom, an alkyl group having from 1 to 4 carbon atoms or a methylthioalkyl group having from 2 to 5 carbon atoms; and R 5 represents a hydrogen atom, is reacted in the presence of a strong acid and in the absence of water with a sulphide of the general formula wherein R represents a hydrogen atom or an alkyl group having up to 3 carbon atoms, thereby to introduce according to the following stipulations one or more methylthioalkyl substituents of the formula(e) CH 3 -S-CHR- wherein R is as above defined: (a) if R 2 , R 3 and R 4 all represented hydrogen atoms, for one of R 3 and R 4 , both of R 3 and R 4 or all of R 3 , R 4 and R 5 , (b) if R 2 represented a methyl group and R 4 represented a hydrogen atom, for R 4 or both of R 4 and R 5 , (c) if R 2 represented a methyl group and R 4 did not represent a hydrogen atom, for R 5 , (d) if R 2 and R 3 both represented hydrogen atoms and R 4 did not represent a hydrogen atom, for R 3 or both of R 3 and R 5 , (e) if R 3 represented a dimethylamino group, for R 5 , (f) if R 3 represented neither a dimethylamino group nor a hydrogen atom and R 4 represented a hydrogen atom, for R 4 or both of R 4 and R 5 , (g) if R 3 represented neither a dimethylamino group nor a hydrogen atom and R<SP>4</SP> did not represent a hydrogen atom, for R 5 , and the methylthioalkyltetracycline derivative is either isolated or demethylthionated by refluxing in a solvent with Raney nickel to give the corresponding alkyltetracycline derivative (in which the or each alkyl substituent is of the formula RCH 2 -). Tetracycline derivatives of the general Formula I wherein R 1 represents a hydrogen atom, a hydroxy group or an acyloxy group having from 1 to 4 carbon atoms; R 2 represents a hydrogen atom or a methyl group; R 3 represents a hydrogen atom, an alkyl group having from 1 to 4 carbon atoms, a methylthioalkyl group having from 2 to 5 carbon atoms or a dimethylamino group; and R 4 and R 5 each represents a hydrogen atom, an alkyl group having from 1 to 4 carbon atoms or a methylthioalkyl group having from 2 to 5 carbon atoms: with the provisos that R 3 and R 4 do not simultaneously represent hydrogen atoms, that when R 2 represents a methyl group R 3 represents a hydrogen atom, that when R 3 represents a dimethylamino group R 4 represents a hydrogen atom and R 5 does not represent a hydrogen atom, and that when R 5 represents a hydrogen atom R 3 and R 4 do not represent (i) a hydrogen atom and a butyl group respectively, or (ii) a methyl group and a butyl group respectively, or (iii) a methyl group and a hydrogen atom respectively, are novel.
GB2627075A 1974-06-25 1975-06-20 Tetracyclines Expired GB1469384A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
IT2435974 1974-06-25

Publications (1)

Publication Number Publication Date
GB1469384A true GB1469384A (en) 1977-04-06

Family

ID=11213252

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2627075A Expired GB1469384A (en) 1974-06-25 1975-06-20 Tetracyclines

Country Status (4)

Country Link
JP (1) JPS5119757A (en)
DE (1) DE2527568A1 (en)
FR (1) FR2279720A1 (en)
GB (1) GB1469384A (en)

Cited By (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
WO2002004407A2 (en) 2000-07-07 2002-01-17 Trustees Of Tufts College 7-substituted tetracycline compounds
US7001918B2 (en) 2001-03-13 2006-02-21 Paratek Pharmaceuticals, Inc. 7-pyrrolyl tetracycline compounds and methods of use thereof
US7056902B2 (en) 2002-01-08 2006-06-06 Paratek Pharmaceuticals, Inc. 4-dedimethylamino tetracycline compounds
US7094806B2 (en) 2000-07-07 2006-08-22 Trustees Of Tufts College 7, 8 and 9-substituted tetracycline compounds
US7323492B2 (en) 2001-08-02 2008-01-29 Paratek Pharmaceuticals, Inc. 7-pyrollyl 9-aminoacyl tetracycline compounds and methods of use thereof
US7326696B2 (en) 2002-03-08 2008-02-05 Paratek Pharmaceuticals, Inc. Amino-methyl substituted tetracycline compounds
US7612053B2 (en) 2000-05-15 2009-11-03 Paratek Pharmaceuticals, Inc. 7-Substituted fused ring tetracycline compounds
US7696186B2 (en) 2001-03-13 2010-04-13 Paratek Pharmaceuticals, Inc. 7,9-substituted tetracycline compounds
US7696187B2 (en) 1999-09-14 2010-04-13 Trustees Of Tufts College Methods of preparing substituted tetracyclines with transition metal-based chemistries
US7820641B2 (en) 2002-03-21 2010-10-26 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds
US7851460B2 (en) 2000-06-16 2010-12-14 Trustees Of Tufts College 7-phenyl-substituted tetracycline compounds
US8048867B2 (en) 2000-07-07 2011-11-01 Trustees Of Tufts College 9-substituted minocycline compounds
US8106225B2 (en) 1999-09-14 2012-01-31 Trustees Of Tufts College Methods of preparing substituted tetracyclines with transition metal-based chemistries
AU2005244988B2 (en) * 2004-05-21 2012-02-02 President And Fellows Of Harvard College Synthesis of tetracyclines and analogues thereof
US8318706B2 (en) 2006-12-21 2012-11-27 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds
US8513223B2 (en) 2006-12-21 2013-08-20 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds for treatment of inflammatory skin disorders
US8518912B2 (en) 2007-11-29 2013-08-27 Actelion Pharmaceuticals Ltd. Phosphonic acid derivates and their use as P2Y12 receptor antagonists
AU2012202559B2 (en) * 2004-05-21 2014-07-17 President And Fellows Of Harvard College Synthesis of tetracyclines and analogues thereof
US9533943B2 (en) 2003-07-09 2017-01-03 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds
EP3354637B1 (en) * 2015-02-13 2021-05-26 Hovione Scientia Limited New polymorphic forms of minocycline base and processes for their preparation

Families Citing this family (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
CA2318580A1 (en) * 1998-01-23 1999-07-29 Mark L. Nelson Pharmaceutically active compounds and methods of use thereof
WO2007117639A2 (en) 2006-04-07 2007-10-18 The President And Fellows Of Harvard College Synthesis of tetracyclines and analogues thereof
US7763735B2 (en) 2006-10-11 2010-07-27 President And Fellows Of Harvard College Synthesis of enone intermediate
US9073829B2 (en) 2009-04-30 2015-07-07 President And Fellows Of Harvard College Synthesis of tetracyclines and intermediates thereto

Cited By (40)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US8106225B2 (en) 1999-09-14 2012-01-31 Trustees Of Tufts College Methods of preparing substituted tetracyclines with transition metal-based chemistries
US7696187B2 (en) 1999-09-14 2010-04-13 Trustees Of Tufts College Methods of preparing substituted tetracyclines with transition metal-based chemistries
US8288570B2 (en) 2000-05-15 2012-10-16 Paratek Pharmaceuticals, Inc. 7-iodo tetracyclines and related methods
US7893282B2 (en) 2000-05-15 2011-02-22 Paratek Pharmaceuticals, Inc. 7-substituted fused ring tetracycline compounds
US7612053B2 (en) 2000-05-15 2009-11-03 Paratek Pharmaceuticals, Inc. 7-Substituted fused ring tetracycline compounds
US7851460B2 (en) 2000-06-16 2010-12-14 Trustees Of Tufts College 7-phenyl-substituted tetracycline compounds
US8168810B2 (en) 2000-06-16 2012-05-01 Trustees Of Tufts College 7-phenyl-substituted tetracycline compounds
US8492365B2 (en) 2000-07-07 2013-07-23 Trustees Of Tufts College 7-substituted tetracycline compounds
US8258120B2 (en) 2000-07-07 2012-09-04 Paratek Pharmaceuticals, Inc. 9-substituted minocycline compounds
US7094806B2 (en) 2000-07-07 2006-08-22 Trustees Of Tufts College 7, 8 and 9-substituted tetracycline compounds
WO2002004407A2 (en) 2000-07-07 2002-01-17 Trustees Of Tufts College 7-substituted tetracycline compounds
US8252777B2 (en) 2000-07-07 2012-08-28 Trustees Of Tufts College 7, 8 and 9-substituted tetracycline compounds
US7696188B2 (en) 2000-07-07 2010-04-13 Trustees Of Tufts College 7,8 and 9-substituted tetracycline compounds
US8048867B2 (en) 2000-07-07 2011-11-01 Trustees Of Tufts College 9-substituted minocycline compounds
US9090541B2 (en) 2000-07-07 2015-07-28 Paratek Pharmaceuticals, Inc. 9-substituted minocycline compounds
AU2001271642B2 (en) * 2000-07-07 2006-01-05 Paratek Pharmaceuticals, Inc. 7-substituted tetracycline compounds
US7875649B2 (en) 2000-07-07 2011-01-25 Trustees Of Tufts College 7, 8 and 9-substituted tetracycline compounds
US6818635B2 (en) 2000-07-07 2004-11-16 Paratek Pharmaceuticals, Inc. 7-substituted tetracycline compounds
WO2002004407A3 (en) * 2000-07-07 2002-04-04 Tufts College 7-substituted tetracycline compounds
EP2289871A1 (en) * 2000-07-07 2011-03-02 Paratek Pharmaceuticals, Inc. 7-substituted tetracycline compounds
US7696186B2 (en) 2001-03-13 2010-04-13 Paratek Pharmaceuticals, Inc. 7,9-substituted tetracycline compounds
US7897784B2 (en) 2001-03-13 2011-03-01 Paratek Pharmaceuticals, Inc. Process for preparing five-membered heterocyclyl tetracycline compounds and methods of use thereof
US7001918B2 (en) 2001-03-13 2006-02-21 Paratek Pharmaceuticals, Inc. 7-pyrrolyl tetracycline compounds and methods of use thereof
US8304445B2 (en) 2001-03-13 2012-11-06 Paratek Pharmaceuticals, Inc. 7-pyrazolyl tetracycline compounds and methods of use thereof
US7696358B2 (en) 2001-03-13 2010-04-13 Paratek Pharmaceuticals, Inc. Five-membered heterocyclyl tetracycline compounds and methods of use thereof
US8211937B2 (en) 2001-08-02 2012-07-03 Paratek Pharmaceuticals, Inc. 7-pyrollyl 9-aminoacyl tetracycline compounds and methods of use thereof
US7323492B2 (en) 2001-08-02 2008-01-29 Paratek Pharmaceuticals, Inc. 7-pyrollyl 9-aminoacyl tetracycline compounds and methods of use thereof
US7056902B2 (en) 2002-01-08 2006-06-06 Paratek Pharmaceuticals, Inc. 4-dedimethylamino tetracycline compounds
US7326696B2 (en) 2002-03-08 2008-02-05 Paratek Pharmaceuticals, Inc. Amino-methyl substituted tetracycline compounds
US7820641B2 (en) 2002-03-21 2010-10-26 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds
US9533943B2 (en) 2003-07-09 2017-01-03 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds
AU2012202559B2 (en) * 2004-05-21 2014-07-17 President And Fellows Of Harvard College Synthesis of tetracyclines and analogues thereof
AU2005244988C1 (en) * 2004-05-21 2012-06-28 President And Fellows Of Harvard College Synthesis of tetracyclines and analogues thereof
AU2005244988B2 (en) * 2004-05-21 2012-02-02 President And Fellows Of Harvard College Synthesis of tetracyclines and analogues thereof
US8513223B2 (en) 2006-12-21 2013-08-20 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds for treatment of inflammatory skin disorders
US9012433B2 (en) 2006-12-21 2015-04-21 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds
US9481639B2 (en) 2006-12-21 2016-11-01 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds for treatment of inflammatory skin disorders
US8318706B2 (en) 2006-12-21 2012-11-27 Paratek Pharmaceuticals, Inc. Substituted tetracycline compounds
US8518912B2 (en) 2007-11-29 2013-08-27 Actelion Pharmaceuticals Ltd. Phosphonic acid derivates and their use as P2Y12 receptor antagonists
EP3354637B1 (en) * 2015-02-13 2021-05-26 Hovione Scientia Limited New polymorphic forms of minocycline base and processes for their preparation

Also Published As

Publication number Publication date
FR2279720B1 (en) 1977-12-02
FR2279720A1 (en) 1976-02-20
DE2527568A1 (en) 1976-01-15
JPS5119757A (en) 1976-02-17

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Legal Events

Date Code Title Description
PS Patent sealed
PCNP Patent ceased through non-payment of renewal fee