GB931560A - Pyrimidones and pyrimidthiones - Google Patents

Pyrimidones and pyrimidthiones

Info

Publication number
GB931560A
GB931560A GB902063A GB902063A GB931560A GB 931560 A GB931560 A GB 931560A GB 902063 A GB902063 A GB 902063A GB 902063 A GB902063 A GB 902063A GB 931560 A GB931560 A GB 931560A
Authority
GB
United Kingdom
Prior art keywords
hydroxy
prepared
compounds
reacting
pyrimidone
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
GB902063A
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.)
Sun Chemical Corp
Original Assignee
Sun Chemical Corp
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 Sun Chemical Corp filed Critical Sun Chemical Corp
Publication of GB931560A publication Critical patent/GB931560A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D239/00Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings
    • C07D239/02Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings
    • C07D239/06Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member
    • C07D239/08Heterocyclic compounds containing 1,3-diazine or hydrogenated 1,3-diazine rings not condensed with other rings having one double bond between ring members or between a ring member and a non-ring member with hetero atoms directly attached in position 2
    • C07D239/10Oxygen or sulfur atoms
    • DTEXTILES; PAPER
    • D06TREATMENT OF TEXTILES OR THE LIKE; LAUNDERING; FLEXIBLE MATERIALS NOT OTHERWISE PROVIDED FOR
    • D06MTREATMENT, NOT PROVIDED FOR ELSEWHERE IN CLASS D06, OF FIBRES, THREADS, YARNS, FABRICS, FEATHERS OR FIBROUS GOODS MADE FROM SUCH MATERIALS
    • D06M15/00Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment
    • D06M15/19Treating fibres, threads, yarns, fabrics, or fibrous goods made from such materials, with macromolecular compounds; Such treatment combined with mechanical treatment with synthetic macromolecular compounds
    • D06M15/37Macromolecular compounds obtained otherwise than by reactions only involving carbon-to-carbon unsaturated bonds
    • D06M15/39Aldehyde resins; Ketone resins; Polyacetals
    • D06M15/423Amino-aldehyde resins

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Textile Engineering (AREA)
  • Treatments For Attaching Organic Compounds To Fibrous Goods (AREA)

Abstract

The invention comprises pyrimidones and pyrimid thiones having the general formula <FORM:0931560/IV(a)/1> wherein X is oxygen or sulphur and Y is hydrogen, hydroxymethyl or an alkoxymethyl group containing not more than 5 carbon atoms. The compounds in which Y represents hydrogen are prepared by reacting urea or thiourea with 2-hydroxy-1,3-diamino propane at an elevated temperature under anhydrous conditions. The dimethyl derivatives are prepared by reacting 5-hydroxy-hexahydro pyrimidone or the corresponding thione with formaldehyde or a formaldehyde-yielding material under alkaline conditions, suitably in aqueous solution at pH 7-12. The alkoxymethyl derivatives are prepared by reacting the dimethylol compounds with a C1-4 alkanol under acidic conditions. Examples describe the preparation of 5-hydroxy hexahydro pyrimidone and its 1,3-dimethylol derivative. The compounds wherein Y is hydroxy- or alkoxy-methyl may be used in crease-proofing cellulosic textiles as described in Specification 931,559 [Group IV(a)].
GB902063A 1958-10-31 1959-10-01 Pyrimidones and pyrimidthiones Expired GB931560A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US77091058A 1958-10-31 1958-10-31

Publications (1)

Publication Number Publication Date
GB931560A true GB931560A (en) 1963-07-17

Family

ID=25090089

Family Applications (2)

Application Number Title Priority Date Filing Date
GB3338159A Expired GB931559A (en) 1958-10-31 1959-10-01 Creaseproofing of cellulosic materials
GB902063A Expired GB931560A (en) 1958-10-31 1959-10-01 Pyrimidones and pyrimidthiones

Family Applications Before (1)

Application Number Title Priority Date Filing Date
GB3338159A Expired GB931559A (en) 1958-10-31 1959-10-01 Creaseproofing of cellulosic materials

Country Status (1)

Country Link
GB (2) GB931559A (en)

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3518043A (en) * 1965-08-17 1970-06-30 Basf Ag Hexahydropyrimidone derivatives and a method of finishing textile material

Cited By (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US3518043A (en) * 1965-08-17 1970-06-30 Basf Ag Hexahydropyrimidone derivatives and a method of finishing textile material

Also Published As

Publication number Publication date
GB931559A (en) 1963-07-17

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