NL7412830A - Werkwijze ter bereiding van (1.3-dihydroxy ubstitueerde en 2.2-digesubstitueerde yloxy (of thio))alkaanzuren. - Google Patents

Werkwijze ter bereiding van (1.3-dihydroxy ubstitueerde en 2.2-digesubstitueerde yloxy (of thio))alkaanzuren.

Info

Publication number
NL7412830A
NL7412830A NL7412830A NL7412830A NL7412830A NL 7412830 A NL7412830 A NL 7412830A NL 7412830 A NL7412830 A NL 7412830A NL 7412830 A NL7412830 A NL 7412830A NL 7412830 A NL7412830 A NL 7412830A
Authority
NL
Netherlands
Prior art keywords
ubstituated
digitually
yloxy
dihydroxy
thio
Prior art date
Application number
NL7412830A
Other languages
English (en)
Dutch (nl)
Original Assignee
Merck & Co Inc
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 Merck & Co Inc filed Critical Merck & Co Inc
Publication of NL7412830A publication Critical patent/NL7412830A/xx

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D333/00—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom
    • C07D333/06—Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings not substituted on the ring sulphur atom with only hydrogen atoms, hydrocarbon or substituted hydrocarbon radicals, directly attached to the ring carbon atoms
    • C07D333/14—Radicals substituted by singly bound hetero atoms other than halogen
    • C07D333/16—Radicals substituted by singly bound hetero atoms other than halogen by oxygen atoms
    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
    • C07C59/00—Compounds having carboxyl groups bound to acyclic carbon atoms and containing any of the groups OH, O—metal, —CHO, keto, ether, groups, groups, or groups
    • C07C59/40—Unsaturated compounds
    • C07C59/58—Unsaturated compounds containing ether groups, groups, groups, or groups
    • C07C59/72—Unsaturated compounds containing ether groups, groups, groups, or groups containing six-membered aromatic rings and other rings

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
NL7412830A 1973-10-12 1974-09-27 Werkwijze ter bereiding van (1.3-dihydroxy ubstitueerde en 2.2-digesubstitueerde yloxy (of thio))alkaanzuren. NL7412830A (nl)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US40596473A 1973-10-12 1973-10-12
US05/492,943 US4006180A (en) 1973-10-12 1974-07-31 [1,3-Dihydroxy-2-substituted and 2,2-disubstituted-indanyloxy(or thio)]alkanoic acids

Publications (1)

Publication Number Publication Date
NL7412830A true NL7412830A (nl) 1975-04-15

Family

ID=27019306

Family Applications (1)

Application Number Title Priority Date Filing Date
NL7412830A NL7412830A (nl) 1973-10-12 1974-09-27 Werkwijze ter bereiding van (1.3-dihydroxy ubstitueerde en 2.2-digesubstitueerde yloxy (of thio))alkaanzuren.

Country Status (8)

Country Link
US (1) US4006180A (xx)
JP (1) JPS5077355A (xx)
DE (1) DE2448393A1 (xx)
DK (1) DK506774A (xx)
FR (1) FR2247217B1 (xx)
GB (1) GB1480239A (xx)
NL (1) NL7412830A (xx)
SE (1) SE7412047L (xx)

Families Citing this family (20)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US5001255A (en) * 1984-12-04 1991-03-19 Sandoz Pharm. Corp. Idene analogs of mevalonolactone and derivatives thereof
US20060258581A1 (en) * 2001-11-21 2006-11-16 Reed John C Methods and composition for derepressions of IAP-inhibited caspase
US20050119176A1 (en) * 2001-11-21 2005-06-02 The Burnham Institute Methods and compositions for derepression of IAP-inhibited caspase
EP1465649A4 (en) * 2001-11-21 2007-07-11 Burnham Inst METHODS AND COMPOSITIONS FOR IAP-INHIBITED CASPASE DERPRESSION (APOPTOSIS PROTEIN INHIBITOR)
US6858615B2 (en) * 2002-02-19 2005-02-22 Parion Sciences, Inc. Phenyl guanidine sodium channel blockers
US6858614B2 (en) * 2002-02-19 2005-02-22 Parion Sciences, Inc. Phenolic guanidine sodium channel blockers
WO2003093258A2 (en) * 2002-05-03 2003-11-13 MAX-PLANCK-Gesellschaft zur Förderung der Wissenschaften e.V. Novel spiro ketone and carboxylic acid derivatives as specific inhibitors for (po3h2) ser/(po3h2)thr-pro-specific peptidyl-prolyl-cis/trans-isomerases
US6903105B2 (en) * 2003-02-19 2005-06-07 Parion Sciences, Inc. Sodium channel blockers
US20050090505A1 (en) * 2003-08-18 2005-04-28 Johnson Michael R. Methods of reducing risk of infection from pathogens
US7745442B2 (en) 2003-08-20 2010-06-29 Parion Sciences, Inc. Methods of reducing risk of infection from pathogens
US20090253714A1 (en) * 2003-08-20 2009-10-08 Johnson Michael R Methods of reducing risk of infection from pathogens
US20070003535A1 (en) * 2005-03-17 2007-01-04 Reed John C Methods and compositions for derepression of IAP-inhibited caspase
US20110183358A1 (en) * 2005-03-17 2011-07-28 The Burnham Institute Methods and compositions for derepression of iap-inhibited caspase
EP1865977A2 (en) * 2005-03-17 2007-12-19 The Burnham Institute for Medical Research Methods and compositions for derepression of iap-inhibited caspase
US20070021439A1 (en) * 2005-07-25 2007-01-25 Parion Sciences, Inc. Methods of reducing risk of infection from pathogens with soluble amide and ester pyrazinoylguanidine sodium channel blockers
US20090043099A1 (en) * 2006-03-17 2009-02-12 The Burnham Institute Methods and compositions for derepression of IAP-inhibited caspase
AR086745A1 (es) 2011-06-27 2014-01-22 Parion Sciences Inc 3,5-diamino-6-cloro-n-(n-(4-(4-(2-(hexil(2,3,4,5,6-pentahidroxihexil)amino)etoxi)fenil)butil)carbamimidoil)pirazina-2-carboxamida
AU2013363215B2 (en) 2012-12-17 2018-03-01 Parion Sciences, Inc. 3,5-diamino-6-chloro-N-(N-(4-phenylbutyl)carbamimidoyl) pyrazine-2- carboxamide compounds
AP2015008556A0 (en) 2012-12-17 2015-06-30 Parion Sciences Inc Chloro-pyrazine carboxamide derivatives useful forthe treatment of diseases favoured by insufficien t mucosal hydration
US9102633B2 (en) 2013-12-13 2015-08-11 Parion Sciences, Inc. Arylalkyl- and aryloxyalkyl-substituted epithelial sodium channel blocking compounds

Family Cites Families (5)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
FR1498459A (xx) * 1965-07-30 1968-01-08
US3704314A (en) * 1968-11-25 1972-11-28 Merck & Co Inc (1-oxo-2-alkylideneindanyloxy) and (1-oxo - 2 - alkylideneindanylthio) alkanoic acids
US3668241A (en) * 1968-11-25 1972-06-06 Merck & Co Inc Substituted 1-oxoinden-5-yloxy alkanoic acids
US3776944A (en) * 1971-09-16 1973-12-04 Warner Lambert Co Tetraloneoxy acetic acids and esters thereof
US3906032A (en) * 1972-11-10 1975-09-16 Squibb & Sons Inc Dihydroxy-tetrahydronaphthyoxyisobutyric acids and alkyl esters and salts thereof

Also Published As

Publication number Publication date
DE2448393A1 (de) 1975-04-17
US4006180A (en) 1977-02-01
FR2247217A1 (xx) 1975-05-09
JPS5077355A (xx) 1975-06-24
SE7412047L (xx) 1975-04-14
FR2247217B1 (xx) 1978-02-03
DK506774A (xx) 1975-06-09
GB1480239A (en) 1977-07-20

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