ES444834A1 - Procedure for the preparation of semicarbazides. (Machine-translation by Google Translate, not legally binding) - Google Patents

Procedure for the preparation of semicarbazides. (Machine-translation by Google Translate, not legally binding)

Info

Publication number
ES444834A1
ES444834A1 ES444834A ES444834A ES444834A1 ES 444834 A1 ES444834 A1 ES 444834A1 ES 444834 A ES444834 A ES 444834A ES 444834 A ES444834 A ES 444834A ES 444834 A1 ES444834 A1 ES 444834A1
Authority
ES
Spain
Prior art keywords
benzenesulfonyl
formula
radical
substituted
see formula
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
ES444834A
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.)
Hoechst AG
Original Assignee
Hoechst AG
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
Priority claimed from DE19702027950 external-priority patent/DE2027950A1/en
Priority claimed from DE19712120266 external-priority patent/DE2120266A1/en
Application filed by Hoechst AG filed Critical Hoechst AG
Publication of ES444834A1 publication Critical patent/ES444834A1/en
Expired legal-status Critical Current

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/435Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having six-membered rings with one nitrogen as the only ring hetero atom
    • A61K31/47Quinolines; Isoquinolines
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D215/00Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems
    • C07D215/02Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms or carbon atoms directly attached to the ring nitrogen atom
    • C07D215/16Heterocyclic compounds containing quinoline or hydrogenated quinoline ring systems having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen atoms 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
    • C07D215/48Carbon atoms having three bonds to hetero atoms with at the most one bond to halogen

Landscapes

  • Chemical & Material Sciences (AREA)
  • Health & Medical Sciences (AREA)
  • Organic Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Epidemiology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Pharmacology & Pharmacy (AREA)
  • General Health & Medical Sciences (AREA)
  • Public Health (AREA)
  • Veterinary Medicine (AREA)
  • Medicinal Chemistry (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

Abstract

Procedure for the preparation of semicarbazides of the formula **(See formula)** where X signifies bidrogen, chlorine, bromine, methyl or methoxy, Y signifies -CH (CH3) -CH2, -, preferably -CH2-CH2-, Z signifies hydrogen or a hydrocarbon radical with 1 or 2 carbon atoms that forms with Y is a 5- or 6-membered anilium, and R means a) a 3 to 7 ring carbon quyleneimino radical that may be optionally unsaturated or substituted by 1 or 2 methyl groups or a lower alcohol group or a methoxy group, b) a pentamethylene imino radical substituted by an endoalkylene radical with 1 to 3 carbon atoms, c) a hexamethylene radical substituted by an endoethylene group in the beta-epsilon position, d) a radical trahydro-isoindoline, 4, 7-endoalkylenehexahydro- or tetrahydro-isoindoline, in which the endoalkylene group contains 1 or 2 carbon atoms and the double bond of the tetrahydroxy compound is in the 5,6 position, and its salts, characterized in that a) benzenesulfonamides are reacted with the formula **(See formula)** conveniently in the form of their salts, with imino-carbamic acid esters, iminothiol-carbamic acid esters or imino-ureas containing the group R- as imino radical, b) amines of the formula RNH2 or their salts are reacted with benzenesulfonyl-isocyanates, benzenesulfonyl-carbamic acid esters, benzenesulfonyl-thiolcarbamic acid esters, benzene sulfonyl-carbamic acid halides or benzenesulfonyl-ureas, substituted in position 3 by group Z and in position 4 by **(See formula)** c) benzenesulfochlorides of the formula are reacted **(See formula)** with R-substituted ureas, d) hydrolyze benzenesulfonyl-isoureas ethers, benzenesulfonyl-isothio-ureas ethers or benzenesulfonyl-imino-parabanic acid derivatives, substituted by R, Z and **(See formula)** or e) is substituted by benzenesulfonyl-thiourcas of the formula **(See formula)** the sulfur atom by an oxygen atom, or f) is introduced into benzenesulfonyl-ureas of the formula **(See formula)** eventually staggered, the radical **(See formula)** and the products according to the invention are optionally treated for the formation of salts with alkaline agents or with acceptable inorganic or organic acids: physiologically. (Machine-translation by Google Translate, not legally binding)
ES444834A 1970-06-06 1976-01-31 Procedure for the preparation of semicarbazides. (Machine-translation by Google Translate, not legally binding) Expired ES444834A1 (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
DE19702027950 DE2027950A1 (en) 1970-06-06 1970-06-06 Benzenesulfonylureas and process for their preparation
DE19712120266 DE2120266A1 (en) 1971-04-26 1971-04-26 Benzenesulfonyl semicarbazides and processes for their preparation

Publications (1)

Publication Number Publication Date
ES444834A1 true ES444834A1 (en) 1977-05-01

Family

ID=25759238

Family Applications (3)

Application Number Title Priority Date Filing Date
ES391792A Expired ES391792A1 (en) 1970-06-06 1971-05-31 Procedure for the preparation of bencenosulfonilureas. (Machine-translation by Google Translate, not legally binding)
ES418120A Expired ES418120A1 (en) 1970-06-06 1973-08-22 Procedure for the preparation of sulfonil-ureas. (Machine-translation by Google Translate, not legally binding)
ES444834A Expired ES444834A1 (en) 1970-06-06 1976-01-31 Procedure for the preparation of semicarbazides. (Machine-translation by Google Translate, not legally binding)

Family Applications Before (2)

Application Number Title Priority Date Filing Date
ES391792A Expired ES391792A1 (en) 1970-06-06 1971-05-31 Procedure for the preparation of bencenosulfonilureas. (Machine-translation by Google Translate, not legally binding)
ES418120A Expired ES418120A1 (en) 1970-06-06 1973-08-22 Procedure for the preparation of sulfonil-ureas. (Machine-translation by Google Translate, not legally binding)

Country Status (15)

Country Link
BE (1) BE768135A (en)
BG (1) BG19796A3 (en)
CA (1) CA986114A (en)
CH (12) CH577974A5 (en)
DK (1) DK138793C (en)
ES (3) ES391792A1 (en)
FI (1) FI50792C (en)
FR (1) FR2100731A1 (en)
HU (1) HU166708B (en)
IE (1) IE35332B1 (en)
IL (1) IL36983A (en)
IT (1) IT1037032B (en)
NL (1) NL7107502A (en)
RO (1) RO58731A (en)
SE (1) SE361038B (en)

Family Cites Families (1)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
DE1294957B (en) * 1966-07-02 1969-05-14 Boehringer & Soehne Gmbh Process for the preparation of hydrindene sulphonylureas and sulphonyl semicarbazides

Also Published As

Publication number Publication date
CH568291A5 (en) 1975-10-31
CH576971A5 (en) 1976-06-30
IT1037032B (en) 1979-11-10
FR2100731A1 (en) 1972-03-24
DK138793C (en) 1979-03-26
IL36983A0 (en) 1971-08-25
CH577478A5 (en) 1976-07-15
BE768135A (en) 1971-12-06
CH577498A5 (en) 1976-07-15
FI50792B (en) 1976-03-31
CH586203A5 (en) 1977-03-31
HU166708B (en) 1975-05-28
RO58731A (en) 1975-12-15
CH586219A5 (en) 1977-03-31
BG19796A3 (en) 1975-10-10
CH580593A5 (en) 1976-10-15
IE35332L (en) 1971-12-06
CH576972A5 (en) 1976-06-30
FR2100731B1 (en) 1974-09-06
CA986114A (en) 1976-03-23
IE35332B1 (en) 1976-01-21
IL36983A (en) 1976-03-31
CH577974A5 (en) 1976-07-30
FI50792C (en) 1976-07-12
ES418120A1 (en) 1976-09-01
NL7107502A (en) 1971-12-08
ES391792A1 (en) 1974-08-01
CH576965A5 (en) 1976-06-30
CH576973A5 (en) 1976-06-30
DK138793B (en) 1978-10-30
SE361038B (en) 1973-10-15
CH577479A5 (en) 1976-07-15

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