GB725945A - Succinimide compounds and method for obtaining the same - Google Patents

Succinimide compounds and method for obtaining the same

Info

Publication number
GB725945A
GB725945A GB2248/53A GB224853A GB725945A GB 725945 A GB725945 A GB 725945A GB 2248/53 A GB2248/53 A GB 2248/53A GB 224853 A GB224853 A GB 224853A GB 725945 A GB725945 A GB 725945A
Authority
GB
United Kingdom
Prior art keywords
chlorophenyl
acid
methyl
obtaining
same
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
GB2248/53A
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.)
Parke Davis and Co LLC
Original Assignee
Parke Davis and Co LLC
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 Parke Davis and Co LLC filed Critical Parke Davis and Co LLC
Publication of GB725945A publication Critical patent/GB725945A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • C07D209/48Iso-indoles; Hydrogenated iso-indoles with oxygen atoms in positions 1 and 3, e.g. phthalimide
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D207/00Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D207/02Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom
    • C07D207/30Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members
    • C07D207/34Heterocyclic compounds containing five-membered rings not condensed with other rings, with one nitrogen atom as the only ring hetero atom with only hydrogen or carbon atoms directly attached to the ring nitrogen atom having two double bonds between ring members or between ring members and non-ring members 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
    • C07D207/36Oxygen or sulfur atoms
    • C07D207/402,5-Pyrrolidine-diones
    • C07D207/4042,5-Pyrrolidine-diones with only hydrogen atoms or radicals containing only hydrogen and carbon atoms directly attached to other ring carbon atoms, e.g. succinimide
    • C07D207/408Radicals containing only hydrogen and carbon atoms attached to ring carbon atoms

Landscapes

  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Pyrrole Compounds (AREA)

Abstract

The invention comprises substituted succinimides of the formula <FORM:0725945/IV (b)/1> wherein R is hydrogen or a methyl radical, and their preparation by reacting a -(o-chlorophenyl)-a -methyl succinic acid or its anhydride with ammonia or methylamine, and heating the intermediate product so obtained (which may be a half-amide, its ammonium or methylamine salt or the mono- or di-salt of the acid, depending upon the quantities of reagents taken) to a temperature between 100 DEG and 350 DEG C. a - (o - Chlorophenyl) - a - methyl succinic acid is prepared from ethyl a -cyano-b -(o-chlorophenyl)-b -methyl acrylate by treatment with ethanolic potassium cyanide followed by acid hydrolysis. The corresponding a - (o - chlorophenyl) - a - methyl succinic anhydride is obtained from the acid using acetyl chloride.
GB2248/53A 1952-02-26 1953-01-26 Succinimide compounds and method for obtaining the same Expired GB725945A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US725945XA 1952-02-26 1952-02-26

Publications (1)

Publication Number Publication Date
GB725945A true GB725945A (en) 1955-03-16

Family

ID=22108607

Family Applications (1)

Application Number Title Priority Date Filing Date
GB2248/53A Expired GB725945A (en) 1952-02-26 1953-01-26 Succinimide compounds and method for obtaining the same

Country Status (1)

Country Link
GB (1) GB725945A (en)

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