ES368323A1 - A procedure for preparing a cosmetic composition. (Machine-translation by Google Translate, not legally binding) - Google Patents

A procedure for preparing a cosmetic composition. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES368323A1
ES368323A1 ES368323A ES368323A ES368323A1 ES 368323 A1 ES368323 A1 ES 368323A1 ES 368323 A ES368323 A ES 368323A ES 368323 A ES368323 A ES 368323A ES 368323 A1 ES368323 A1 ES 368323A1
Authority
ES
Spain
Prior art keywords
radical
formula
hydrogen atom
representing
free amino
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
ES368323A
Other languages
Spanish (es)
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.)
LOreal SA
Original Assignee
LOreal SA
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 LOreal SA filed Critical LOreal SA
Publication of ES368323A1 publication Critical patent/ES368323A1/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07KPEPTIDES
    • C07K1/00General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length
    • C07K1/006General methods for the preparation of peptides, i.e. processes for the organic chemical preparation of peptides or proteins of any length of peptides containing derivatised side chain amino acids
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/40Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing nitrogen
    • A61K8/44Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof
    • A61K8/447Aminocarboxylic acids or derivatives thereof, e.g. aminocarboxylic acids containing sulfur; Salts; Esters or N-acylated derivatives thereof containing sulfur
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4906Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom
    • A61K8/4926Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with one nitrogen as the only hetero atom having six membered rings
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K8/00Cosmetics or similar toiletry preparations
    • A61K8/18Cosmetics or similar toiletry preparations characterised by the composition
    • A61K8/30Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds
    • A61K8/49Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds
    • A61K8/4986Cosmetics or similar toiletry preparations characterised by the composition containing organic compounds containing heterocyclic compounds with sulfur as the only hetero atom
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61QSPECIFIC USE OF COSMETICS OR SIMILAR TOILETRY PREPARATIONS
    • A61Q19/00Preparations for care of the skin
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/04Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D213/60Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom with hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D213/78Carbon atoms having three bonds to hetero atoms, with at the most one bond to halogen, e.g. ester or nitrile radicals
    • C07D213/81Amides; Imides
    • C07D213/82Amides; Imides in position 3
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D213/00Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
    • C07D213/02Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
    • C07D213/89Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members with hetero atoms directly attached to the ring nitrogen atom
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D333/00Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom
    • C07D333/02Heterocyclic compounds containing five-membered rings having one sulfur atom as the only ring hetero atom not condensed with other rings
    • C07D333/04Heterocyclic 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
    • C07D333/26Heterocyclic 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 hetero atoms or with carbon atoms having three bonds to hetero atoms with at the most one bond to halogen, e.g. ester or nitrile radicals, directly attached to ring carbon atoms
    • C07D333/30Hetero atoms other than halogen
    • C07D333/34Sulfur atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Health & Medical Sciences (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • General Health & Medical Sciences (AREA)
  • Animal Behavior & Ethology (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Birds (AREA)
  • Epidemiology (AREA)
  • Biochemistry (AREA)
  • Biophysics (AREA)
  • Genetics & Genomics (AREA)
  • Medicinal Chemistry (AREA)
  • Molecular Biology (AREA)
  • Proteomics, Peptides & Aminoacids (AREA)
  • Analytical Chemistry (AREA)
  • Dermatology (AREA)
  • Cosmetics (AREA)
  • Acyclic And Carbocyclic Compounds In Medicinal Compositions (AREA)

Abstract

Method of preparing a cosmetic composition, characterized in that, in an appropriate cosmetic vehicle at a temperature close to room temperature and at the same time as stirring, at least one active compound taken from the group consisting of: (a) the compounds is added of formula I below: **(See formula)** in which R represents the radical (C6H5) 3-C-, the radical (C6-H5) 2-CH, the radical C6H5-CH2-, or finally the radical HOOO- (CH2) n-, where n is an integer less than or equal to 4, preferably equal to 1 or 2, and R'represents a hydrogen atom or a radical COR''or SO2R''with R''representing an alcohol radical or an aryl radical, (b) the compounds of formula II below: **(See formula)** in which: R1 and R2 represent a hydrogen atom or a lower alcohol radical, R1 and R2 may be identical or different, R3 represents the radical of formula (CH2) p-R4, in which R4 represents: -C6H5; or CHOH-CH2 - H + (CH3) 3 Cl- or COOR5, (R5 representing a hydrogen atom or a lower alcohol radical) or the terbutyl-C (CH5) 3 radical; or the trityl-C (C6H5) 3 radical; or -CH2-NH2 or **(See formula)** or the thienyl radical: **(See formula)** or also the radical (H-oxypyridyl) -2 **(See formula)** p equals 0 to 1 or 2; n equals 0 or 1; and R'represents a hydrogen atom or a radical COR''or SO2R'', R''representing an alcohol radical or an aryl radical; (c) the compounds of formula III below: R - S - CH2 - CH2 - NH - R'(III) in which R represents a hydrocarbon radical having up to 20 carbon atoms, saturated or unsaturated, linear or branched, which may optionally comprise 1 or more heteroatoms and one or more alcohol functions, one of which may be terminal, and R'represents a hydrogen atom or a radical COR'' or SO2R'' with R'' representing an alcohol radical or an aryl radical; (d) the compounds of formula IV below: **(See formula)** in which: n is 0 or 1, R1 and R2 identical or different represent a hydrogen atom or a lower alcohol radical, R represents the group of formula: - (CH2) p-R6 (where p is equal to 0.1 or 2) in which R6 represents: -C6H5 or -COOR (R representing a lower alcohol radical) or - (CH3) 3 or -C (C6H5) 3 or **(See formula)** (R7 representing a hydrogen atom or an acyl or sulfonyl radical, R8 representing a lower alcohol radical or a hydrogen atom only when R7 represents a hydrogen atom) or -CH2-NH-R7 or the thienyl-2 radical of formula **(See formula)** or a linear or branched, saturated or unsaturated, hydrocarbon radical comprising up to 20 carbon atoms and possibly having in its chain one or more heteroatoms and one or more alcohol functions, one of which may be terminal; R4 represents: a hydrogen atom, in which case R5 represents a radical - (CH2) m-CO2H, where m is an integer ranging from 1 to 5, and y is = 1 and x = 1, if R3 does not comprise any group free amino, y = 2 and x = 1, if R3 comprises a free amino group; or an acyl or sulfonyl radical, in which case R5 can be: equal to (C6H5) 3C-, (C6H5) 2CH-, C6H5-Ch2-, y = 1 and x = 1, if R3 does not comprise any free amino group, and = 2 and x = 1, if R3, comprises a free amino group, or equal to - (CH2) m-CO2H, y = 1 and x = 1, if R3, comprises a free amino group, y = 1 and x = 2, if R3 does not comprise any free amino group. (Machine-translation by Google Translate, not legally binding)
ES368323A 1968-06-14 1969-06-13 A procedure for preparing a cosmetic composition. (Machine-translation by Google Translate, not legally binding) Expired ES368323A1 (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US73696068A 1968-06-14 1968-06-14

Publications (1)

Publication Number Publication Date
ES368323A1 true ES368323A1 (en) 1971-06-16

Family

ID=24962038

Family Applications (1)

Application Number Title Priority Date Filing Date
ES368323A Expired ES368323A1 (en) 1968-06-14 1969-06-13 A procedure for preparing a cosmetic composition. (Machine-translation by Google Translate, not legally binding)

Country Status (8)

Country Link
JP (1) JPS5022096B1 (en)
BE (1) BE733993A (en)
CA (1) CA930669A (en)
CH (1) CH534515A (en)
DE (1) DE1930023A1 (en)
ES (1) ES368323A1 (en)
FR (1) FR2011940A1 (en)
NL (1) NL6909079A (en)

Families Citing this family (7)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
LU63057A1 (en) * 1971-04-23 1972-12-11 Oreal
LU76148A1 (en) * 1976-11-08 1978-07-10
FR2455457A1 (en) * 1979-05-03 1980-11-28 Oreal COMPOSITIONS CONTAINING CERTAIN N-OXYPYRIDYL-2-THIOL DERIVATIVES FOR THE STRENGTHENING AND REVITALIZATION OF FRAGILE OR ALTERED NAILS
FR2462159A1 (en) * 1979-08-02 1981-02-13 Oreal Strengthening and revitalising brittle finger nails - using an inorganic or organic salt of benzyl-2-thio:ethylamine
FR2740340B1 (en) * 1995-10-30 1997-12-05 Oreal USE OF CARBOXYLIC ACIDS CARRYING A SULFURED FUNCTION TO PROMOTE SKIN DEQUAMATION OR STIMULATE EPIDERMAL RENEWAL
ITMI20020510A1 (en) * 2002-03-11 2003-09-11 Ghisalberti Carlo TOPICAL COMPOSITIONS CONTAINING L-CISTEIN DERIVATIVES
CN115501125A (en) * 2022-10-20 2022-12-23 澳门科技大学 H for repairing skin lesions 2 S donor gel and H 2 Preparation method of S donor gel

Family Cites Families (4)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB1051870A (en) * 1964-01-29
NL131093C (en) * 1965-12-22
CH514335A (en) * 1967-06-21 1971-10-31 Oreal Cosmetic composition for improving the appearance of hair tending to have a greasy appearance
NL144484B (en) * 1967-07-26 1975-01-15 Merck & Co Inc PROCESS FOR THE PREPARATION OF A MEDICINAL PRODUCT WITH ANTI-ANFLAMMATORY ACTION AND A PROCESS FOR THE PREPARATION OF THE ANTI-INFLAMMATORY ACTIVE ARALKYL MERCAPTOAMINO ACIDS.

Also Published As

Publication number Publication date
FR2011940B1 (en) 1974-08-09
CH534515A (en) 1973-03-15
JPS5022096B1 (en) 1975-07-28
BE733993A (en) 1969-12-03
NL6909079A (en) 1969-12-16
CA930669A (en) 1973-07-24
DE1930023A1 (en) 1970-01-15
FR2011940A1 (en) 1970-03-13

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