ES442483A1 - Procedimiento para la preparacion de (1-alcohil -5-nitro-i- midazolil-2 - alcohil)-heteroaril-sulfuros. - Google Patents

Procedimiento para la preparacion de (1-alcohil -5-nitro-i- midazolil-2 - alcohil)-heteroaril-sulfuros.

Info

Publication number: ES442483A1
Authority: ES; Spain
Prior art keywords: formula; nitro; see; see formula; alcohol
Prior art date: 1974-11-15
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

ES442483A

Other languages

English (en)

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.)

1974-11-15

Filing date

1975-11-10

Publication date

1977-04-01

1974-11-15 Priority claimed from DE19742454728 external-priority patent/DE2454728A1/de

1974-11-23 Priority claimed from DE19742455582 external-priority patent/DE2455582A1/de

1975-11-10 Application filed by Hoechst AG filed Critical Hoechst AG

1977-04-01 Publication of ES442483A1 publication Critical patent/ES442483A1/es

Status Expired legal-status Critical Current

Links

125000002496 methyl group Chemical group [H]C([H])([H])* 0.000 abstract 5
125000000449 nitro group Chemical group [O-][N+](*)=O 0.000 abstract 5
125000004093 cyano group Chemical group *C#N 0.000 abstract 4
RAXXELZNTBOGNW-UHFFFAOYSA-N imidazole Natural products C1=CNC=N1 RAXXELZNTBOGNW-UHFFFAOYSA-N 0.000 abstract 3
WKBOTKDWSSQWDR-UHFFFAOYSA-N Bromine atom Chemical compound [Br] WKBOTKDWSSQWDR-UHFFFAOYSA-N 0.000 abstract 2
ZAMOUSCENKQFHK-UHFFFAOYSA-N Chlorine atom Chemical compound [Cl] ZAMOUSCENKQFHK-UHFFFAOYSA-N 0.000 abstract 2
PXGOKWXKJXAPGV-UHFFFAOYSA-N Fluorine Chemical compound FF PXGOKWXKJXAPGV-UHFFFAOYSA-N 0.000 abstract 2
229910052783 alkali metal Inorganic materials 0.000 abstract 2
150000001340 alkali metals Chemical class 0.000 abstract 2
GDTBXPJZTBHREO-UHFFFAOYSA-N bromine Substances BrBr GDTBXPJZTBHREO-UHFFFAOYSA-N 0.000 abstract 2
229910052794 bromium Inorganic materials 0.000 abstract 2
229910052801 chlorine Inorganic materials 0.000 abstract 2
239000000460 chlorine Substances 0.000 abstract 2
229910052731 fluorine Inorganic materials 0.000 abstract 2
239000011737 fluorine Substances 0.000 abstract 2
229910052736 halogen Inorganic materials 0.000 abstract 2
150000002367 halogens Chemical group 0.000 abstract 2
229910052739 hydrogen Inorganic materials 0.000 abstract 2
239000001257 hydrogen Substances 0.000 abstract 2
PNDPGZBMCMUPRI-UHFFFAOYSA-N iodine Chemical compound II PNDPGZBMCMUPRI-UHFFFAOYSA-N 0.000 abstract 2
125000000956 methoxy group Chemical group [H]C([H])([H])O* 0.000 abstract 2
-1 nitrobenzoyl Chemical group 0.000 abstract 2
125000002924 primary amino group Chemical group [H]N([H])* 0.000 abstract 2
JYEUMXHLPRZUAT-UHFFFAOYSA-N 1,2,3-triazine Chemical group C1=CN=NN=C1 JYEUMXHLPRZUAT-UHFFFAOYSA-N 0.000 abstract 1
QGZKDVFQNNGYKY-UHFFFAOYSA-O Ammonium Chemical compound [NH4+] QGZKDVFQNNGYKY-UHFFFAOYSA-O 0.000 abstract 1
UFHFLCQGNIYNRP-UHFFFAOYSA-N Hydrogen Chemical compound [H][H] UFHFLCQGNIYNRP-UHFFFAOYSA-N 0.000 abstract 1
DGAQECJNVWCQMB-PUAWFVPOSA-M Ilexoside XXIX Chemical compound C[C@@H]1CC[C@@]2(CC[C@@]3(C(=CC[C@H]4[C@]3(CC[C@@H]5[C@@]4(CC[C@@H](C5(C)C)OS(=O)(=O)[O-])C)C)[C@@H]2[C@]1(C)O)C)C(=O)O[C@H]6[C@@H]([C@H]([C@@H]([C@H](O6)CO)O)O)O.[Na+] DGAQECJNVWCQMB-PUAWFVPOSA-M 0.000 abstract 1
ZCQWOFVYLHDMMC-UHFFFAOYSA-N Oxazole Chemical compound C1=COC=N1 ZCQWOFVYLHDMMC-UHFFFAOYSA-N 0.000 abstract 1
ZLMJMSJWJFRBEC-UHFFFAOYSA-N Potassium Chemical compound [K] ZLMJMSJWJFRBEC-UHFFFAOYSA-N 0.000 abstract 1
WTKZEGDFNFYCGP-UHFFFAOYSA-N Pyrazole Chemical compound C=1C=NNC=1 WTKZEGDFNFYCGP-UHFFFAOYSA-N 0.000 abstract 1
JUJWROOIHBZHMG-UHFFFAOYSA-N Pyridine Chemical group C1=CC=NC=C1 JUJWROOIHBZHMG-UHFFFAOYSA-N 0.000 abstract 1
CZPWVGJYEJSRLH-UHFFFAOYSA-N Pyrimidine Chemical compound C1=CN=CN=C1 CZPWVGJYEJSRLH-UHFFFAOYSA-N 0.000 abstract 1
FZWLAAWBMGSTSO-UHFFFAOYSA-N Thiazole Chemical compound C1=CSC=N1 FZWLAAWBMGSTSO-UHFFFAOYSA-N 0.000 abstract 1
150000003863 ammonium salts Chemical class 0.000 abstract 1
125000004122 cyclic group Chemical group 0.000 abstract 1
125000000113 cyclohexyl group Chemical group [H]C1([H])C([H])([H])C([H])([H])C([H])(*)C([H])([H])C1([H])[H] 0.000 abstract 1
125000001495 ethyl group Chemical group [H]C([H])([H])C([H])([H])* 0.000 abstract 1
125000000623 heterocyclic group Chemical group 0.000 abstract 1
150000002431 hydrogen Chemical class 0.000 abstract 1
229910052740 iodine Inorganic materials 0.000 abstract 1
125000000959 isobutyl group Chemical group [H]C([H])([H])C([H])(C([H])([H])[H])C([H])([H])* 0.000 abstract 1
125000001449 isopropyl group Chemical group [H]C([H])([H])C([H])(*)C([H])([H])[H] 0.000 abstract 1
MYWUZJCMWCOHBA-VIFPVBQESA-N methamphetamine Chemical compound CN[C@@H](C)CC1=CC=CC=C1 MYWUZJCMWCOHBA-VIFPVBQESA-N 0.000 abstract 1
238000000034 method Methods 0.000 abstract 1
125000006502 nitrobenzyl group Chemical group 0.000 abstract 1
WCPAKWJPBJAGKN-UHFFFAOYSA-N oxadiazole Chemical compound C1=CON=N1 WCPAKWJPBJAGKN-UHFFFAOYSA-N 0.000 abstract 1
CQDAMYNQINDRQC-UHFFFAOYSA-N oxatriazole Chemical compound C1=NN=NO1 CQDAMYNQINDRQC-UHFFFAOYSA-N 0.000 abstract 1
125000001997 phenyl group Chemical group [H]C1=C([H])C([H])=C(*)C([H])=C1[H] 0.000 abstract 1
229910052700 potassium Inorganic materials 0.000 abstract 1
239000011591 potassium Substances 0.000 abstract 1
125000003373 pyrazinyl group Chemical group 0.000 abstract 1
PBMFSQRYOILNGV-UHFFFAOYSA-N pyridazine Chemical compound C1=CC=NN=C1 PBMFSQRYOILNGV-UHFFFAOYSA-N 0.000 abstract 1
229910052708 sodium Inorganic materials 0.000 abstract 1
239000011734 sodium Substances 0.000 abstract 1
229960002317 succinimide Drugs 0.000 abstract 1
150000003536 tetrazoles Chemical group 0.000 abstract 1
VLLMWSRANPNYQX-UHFFFAOYSA-N thiadiazole Chemical compound C1=CSN=N1.C1=CSN=N1 VLLMWSRANPNYQX-UHFFFAOYSA-N 0.000 abstract 1
YGNGABUJMXJPIJ-UHFFFAOYSA-N thiatriazole Chemical group C1=NN=NS1 YGNGABUJMXJPIJ-UHFFFAOYSA-N 0.000 abstract 1
150000003852 triazoles Chemical class 0.000 abstract 1

Classifications

- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D417/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00
- C07D417/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings
- C07D417/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and sulfur atoms as the only ring hetero atoms, not provided for by group C07D415/00 containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D401/00—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
- C07D401/02—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings
- C07D401/12—Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom containing two hetero rings linked by a chain containing hetero atoms as chain links
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D413/00—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms
- C07D413/02—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings
- C07D413/12—Heterocyclic compounds containing two or more hetero rings, at least one ring having nitrogen and oxygen atoms as the only ring hetero atoms containing two hetero rings linked by a chain containing hetero atoms as chain links

Landscapes

Chemical & Material Sciences (AREA)
Organic Chemistry (AREA)
Plural Heterocyclic Compounds (AREA)
Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)

ES442483A 1974-11-15 1975-11-10 Procedimiento para la preparacion de (1-alcohil -5-nitro-i- midazolil-2 - alcohil)-heteroaril-sulfuros. Expired ES442483A1 (es)

Applications Claiming Priority (2)

Application Number	Priority Date	Filing Date	Title
DE19742454728 DE2454728A1 (de)	1974-11-15	1974-11-15	Verfahren zur herstellung von (1alkyl-5-nitro-imidazolyl-2-alkyl)-heteroaryl-sulfiden
DE19742455582 DE2455582A1 (de)	1974-11-23	1974-11-23	Verfahren zur herstellung von (1-alkyl-5-nitro-imidazolyl-2-alkyl)heteroaryl-sulfiden

Publications (1)

Publication Number	Publication Date
ES442483A1 true ES442483A1 (es)	1977-04-01

Family

ID=25767992

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES442483A Expired ES442483A1 (es)	1974-11-15	1975-11-10	Procedimiento para la preparacion de (1-alcohil -5-nitro-i- midazolil-2 - alcohil)-heteroaril-sulfuros.

Country Status (6)

Country	Link
JP (1)	JPS51125285A (da)
DK (1)	DK514475A (da)
ES (1)	ES442483A1 (da)
FR (1)	FR2291201A1 (da)
LU (1)	LU73798A1 (da)
NL (1)	NL7513132A (da)

1975
- 1975-11-10 NL NL7513132A patent/NL7513132A/xx unknown
- 1975-11-10 ES ES442483A patent/ES442483A1/es not_active Expired
- 1975-11-13 LU LU73798A patent/LU73798A1/xx unknown
- 1975-11-14 DK DK514475A patent/DK514475A/da unknown
- 1975-11-15 JP JP50137711A patent/JPS51125285A/ja active Pending
- 1975-11-17 FR FR7535007A patent/FR2291201A1/fr not_active Withdrawn

Also Published As

Publication number	Publication date
LU73798A1 (da)	1976-09-06
NL7513132A (nl)	1976-05-18
DK514475A (da)	1976-05-16
JPS51125285A (en)	1976-11-01
FR2291201A1 (fr)	1976-06-11

Publication	Publication Date	Title
ES8302010A1 (es)	1983-01-01	Un procedimiento para la preparacion de un derivado de n- arilbenzamida
ES8505652A1 (es)	1985-06-01	Procedimiento para preparar nuevas 1-bencil-aminoalquil-pirrolidinonas
ES442483A1 (es)	1977-04-01	Procedimiento para la preparacion de (1-alcohil -5-nitro-i- midazolil-2 - alcohil)-heteroaril-sulfuros.
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ES425373A1 (es)	1976-09-01	Procedimiento para la produccion de pirazolonas-(5) 1-sus- tituidas.
ES460083A1 (es)	1978-10-01	Un procedimiento para la preparacion de nuevos compuestos deacidos 2-alquil(inferior)-2 o 3-cefem-4-carboxilicos-7-sus- tituidos.
ES438234A1 (es)	1977-05-16	Un procedimiento para la preparacion de derivados de oxici- clohexano.
ES423233A1 (es)	1976-07-01	Procedimiento para la preparacion de nuevas 2-fenilamino- imidazolinas-(2) sustituidas.
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ES8507450A1 (es)	1985-09-16	Un procedimiento para la preparacion de nuevos derivados de difeniletanona.
GB1506022A (en)	1978-04-05	1-acyl-4-(o-halophenyl)thiosemicarbazides
ES475596A1 (es)	1979-12-01	Procedimiento para la preparacion de derivados de fenoxial- canolaminas
ES431552A1 (es)	1977-02-01	Procedimiento para preparar triazinadionas herbicidas.
ES406098A1 (es)	1976-03-01	Procedimiento para la obtencion de derivados de 2,6-dini- tro-3,4-xilidena.
SE436870B (sv)	1985-01-28	Sett att framstella nya n-substituerade kanelsyraamider
CH614932A5 (en)	1979-12-28	Process for the preparation of new terpenoaromatic amidines
US2478146A (en)	1949-08-02	Benzenesulfonylthiazoles and preparation of the same
ES439049A1 (es)	1977-05-16	Un procedimiento para preparar compuestos de sulfonilbenci- midazol.
ES322851A1 (es)	1967-01-01	Procedimiento para la sintesis de derivados basicos de dihidro-1,3-benzoxacin-2,4-diona.
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ES458042A1 (es)	1978-08-16	Nuevo procedimiento para la sintesis de la 1-ciano-2-metil- 3-(2-(((5-metil-imidazol-4-il-)metil)tio)etil)-guanidina.
GB1353581A (en)	1974-05-22	Process for preparing triazine derivatives
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ES351343A1 (es)	1969-06-01	Un procedimiento para la preparacion de derivados de benzo-diacepina.
JPS5651467A (en)	1981-05-09	Manufacture of 552222trihalogenoethyl444 dialkylltetrahydrofurann22one and iminium salt thereof