ES418120A1 - Procedure for the preparation of sulfonil-ureas. (Machine-translation by Google Translate, not legally binding) - Google Patents

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

Info

Publication number
ES418120A1
ES418120A1 ES418120A ES418120A ES418120A1 ES 418120 A1 ES418120 A1 ES 418120A1 ES 418120 A ES418120 A ES 418120A ES 418120 A ES418120 A ES 418120A ES 418120 A1 ES418120 A1 ES 418120A1
Authority
ES
Spain
Prior art keywords
carbon atoms
benzenesulfonyl
formula
salts
substituted
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
ES418120A
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
Farbwerke 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, Farbwerke Hoechst AG filed Critical Hoechst AG
Publication of ES418120A1 publication Critical patent/ES418120A1/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 sulfonylureas of the formula **(See formula)** where X means hydrogen, chlorine, bromine, methoxy or methyl, Y means -CH (CH3) -CH2-, -CH2-CH (CH3) - or, preferably, -CH2-CH2-, R means, a) alcohol with 3 to 6 carbon atoms, b) cycloalkyl with 5 to 8 carbon atoms, which may be optionally substituted by 1 or 2 alcohol groups with a total of 3 carbon atoms or chlorine, c) cycloalkenyl with 5 to 8 carbon atoms which may optionally be replaced by a total of 3 carbon atoms, d) bicycloalkoxy or bicycloalkenyl with 7 to 8 carbon atoms, e) nortricicycl, f) spiro [2,4] -heptyl, and z means hydrogen or a hydrocarbon radical with 1 or 2 carbon atoms that form with Y a 5- or 6-membered ring and its salts, characterized in that a) benzenesulfonyl-isocyanates, benzenesulfonyl-carbamic acid esters, benzenesulfonyl-thiolcarbamic acid esters, benzenesulfonylureas are reacted, - semicarbazides or -semicarbazones substituted in position 4 with the group **(See formula)** or in position 3 with group Z with an amine R-NH2 or its salts, or sulfonamides of the formula are reacted **(See formula)** or its salts, with isocyanates, esters of carbamic acid, esters of thiolcarbamic acid, halides of carbamic acid or ureas, E-substituted; or b) suitably substituted benzenesulfonyl iso-urea-ethers, -isourea-esters, -isothiourea-ethers, benzenesulfonylparabanic acids or benzenesulfonyl-haloformic acid amidines, or compounds of the formula **(See formula)** wherein U means low molecular weight O-alcohol, low molecular weight S-alcohol or halogen (preferably chlorine); or c) in suitably substituted benzenesulfonyl-thiorureas, thioamidoalcohyl-benzenesulfonylureas or thioamidoaleohyl-benzenesulphonylthioureas, the sulfur atom or the sulfur atoms of the thiourea group and/or of the thioamido group is replaced by an oxygen atom or or suitably substituted carbodiimides are subjected to addition with water, or d) suitable benzenesulfinylureas or benzenesulfenylureas are oxidized, or e) in benzenesulfonylureas of the formula **(See formula)** the radical is introduced by acylation, optionally in stages. f) suitably substituted benzenesulfonyl halides are reacted with R-substituted ureas or their alkali metal salts, or suitably substituted benzenesulfinic acid halides or, in the presence of acidic condensing agents, also suitably substituted sulfinic acids or their salts are reacted of alkali metals, with NR-N'-hydroxy-urea; and the reaction products are optionally treated with alkaline agents for the formation of salts. (Machine-translation by Google Translate, not legally binding)
ES418120A 1970-06-06 1973-08-22 Procedure for the preparation of sulfonil-ureas. (Machine-translation by Google Translate, not legally binding) Expired ES418120A1 (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
ES418120A1 true ES418120A1 (en) 1976-09-01

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 (1)

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)

Family Applications After (1)

Application Number Title Priority Date Filing Date
ES444834A Expired ES444834A1 (en) 1970-06-06 1976-01-31 Procedure for the preparation of semicarbazides. (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
ES444834A1 (en) 1977-05-01
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
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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