ES312479A1 - Un procedimiento para la preparacion de n- (4- (beta-fenoxiacetamidoetil) -bencenosulfonil) -n'-ciclohexilurea - Google Patents

Un procedimiento para la preparacion de n- (4- (beta-fenoxiacetamidoetil) -bencenosulfonil) -n'-ciclohexilurea

Info

Publication number: ES312479A1
Authority: ES; Spain
Prior art keywords: beta; ethyl; phenoxyacetamido; benzenesulfonyl; cyclohexyl
Prior art date: 1963-10-19
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

ES0312479A

Other languages

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.)

1963-10-19

Filing date

1965-04-30

Publication date

1966-04-01

1965-04-30 Application filed by Hoechst AG, Farbwerke Hoechst AG filed Critical Hoechst AG

1966-04-01 Publication of ES312479A1 publication Critical patent/ES312479A1/es

Status Expired legal-status Critical Current

Links

-1 beta-phenoxyacetamidoethyl Chemical group 0.000 title abstract 9
238000000034 method Methods 0.000 title abstract 3
150000003839 salts Chemical class 0.000 abstract 4
239000002253 acid Substances 0.000 abstract 3
150000007513 acids Chemical class 0.000 abstract 2
PAFZNILMFXTMIY-UHFFFAOYSA-N cyclohexylamine Chemical compound NC1CCCCC1 PAFZNILMFXTMIY-UHFFFAOYSA-N 0.000 abstract 2
150000002148 esters Chemical class 0.000 abstract 2
PKJVUQYJUYBPIW-UHFFFAOYSA-N 2-phenoxy-n-[2-(4-sulfamoylphenyl)ethyl]acetamide Chemical compound C1=CC(S(=O)(=O)N)=CC=C1CCNC(=O)COC1=CC=CC=C1 PKJVUQYJUYBPIW-UHFFFAOYSA-N 0.000 abstract 1
PUUPUUMOXPWVIJ-UHFFFAOYSA-N N-[2-[4-(cyclohexylcarbamoylsulfamoyl)phenyl]ethyl]-2-phenoxyacetamide Chemical compound O(C1=CC=CC=C1)CC(=O)NCCC1=CC=C(C=C1)S(=O)(=O)NC(=O)NC1CCCCC1 PUUPUUMOXPWVIJ-UHFFFAOYSA-N 0.000 abstract 1
LFUHSJPXEHAOKE-UHFFFAOYSA-N O(C1=CC=CC=C1)CC(=O)NCCC1=CC=C(C=C1)S(=O)(=O)Cl Chemical compound O(C1=CC=CC=C1)CC(=O)NCCC1=CC=C(C=C1)S(=O)(=O)Cl LFUHSJPXEHAOKE-UHFFFAOYSA-N 0.000 abstract 1
GYUVVQOEYLCOMZ-UHFFFAOYSA-N O(C1=CC=CC=C1)CC(=O)NCCC1=CC=C(C=C1)S(=O)(=O)N=C=O Chemical compound O(C1=CC=CC=C1)CC(=O)NCCC1=CC=C(C=C1)S(=O)(=O)N=C=O GYUVVQOEYLCOMZ-UHFFFAOYSA-N 0.000 abstract 1
JBSHMHMKIMIGCT-UHFFFAOYSA-N O(C1=CC=CC=C1)CC(=O)NCCC1=CC=C(C=C1)S(=O)(=O)NC(O)=O Chemical compound O(C1=CC=CC=C1)CC(=O)NCCC1=CC=C(C=C1)S(=O)(=O)NC(O)=O JBSHMHMKIMIGCT-UHFFFAOYSA-N 0.000 abstract 1
PWVNDBHVOACXBF-UHFFFAOYSA-N O(C1=CC=CC=C1)CC(=O)NCCC1=CC=C(C=C1)SNC(=O)NC1CCCCC1 Chemical compound O(C1=CC=CC=C1)CC(=O)NCCC1=CC=C(C=C1)SNC(=O)NC1CCCCC1 PWVNDBHVOACXBF-UHFFFAOYSA-N 0.000 abstract 1
230000010933 acylation Effects 0.000 abstract 1
238000005917 acylation reaction Methods 0.000 abstract 1
NNHSFBDNDJBVBD-UHFFFAOYSA-N benzenesulfinylurea Chemical compound NC(=O)NS(=O)C1=CC=CC=C1 NNHSFBDNDJBVBD-UHFFFAOYSA-N 0.000 abstract 1
230000015572 biosynthetic process Effects 0.000 abstract 1
238000006243 chemical reaction Methods 0.000 abstract 1
239000003795 chemical substances by application Substances 0.000 abstract 1
KQWGXHWJMSMDJJ-UHFFFAOYSA-N cyclohexyl isocyanate Chemical compound O=C=NC1CCCCC1 KQWGXHWJMSMDJJ-UHFFFAOYSA-N 0.000 abstract 1
OQQXGCLLMDQESN-UHFFFAOYSA-N cyclohexylcarbamic acid Chemical class OC(=O)NC1CCCCC1 OQQXGCLLMDQESN-UHFFFAOYSA-N 0.000 abstract 1
HKRSMZNXQYMWPW-UHFFFAOYSA-N cyclohexylcarbamothioic s-acid Chemical class SC(=O)NC1CCCCC1 HKRSMZNXQYMWPW-UHFFFAOYSA-N 0.000 abstract 1
WUESWDIHTKHGQA-UHFFFAOYSA-N cyclohexylurea Chemical compound NC(=O)NC1CCCCC1 WUESWDIHTKHGQA-UHFFFAOYSA-N 0.000 abstract 1
150000002170 ethers Chemical class 0.000 abstract 1
NYLHFSLGOJDWNQ-UHFFFAOYSA-N n-[4-(2-azaniumylethyl)phenyl]sulfonyl-n'-cyclohexylcarbamimidate Chemical compound C1=CC(CCN)=CC=C1S(=O)(=O)NC(=O)NC1CCCCC1 NYLHFSLGOJDWNQ-UHFFFAOYSA-N 0.000 abstract 1
125000004430 oxygen atom Chemical group O* 0.000 abstract 1
125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 1
229910052717 sulfur Inorganic materials 0.000 abstract 1
125000004434 sulfur atom Chemical group 0.000 abstract 1

Landscapes

Organic Low-Molecular-Weight Compounds And Preparation Thereof (AREA)

ES0312479A 1963-10-19 1965-04-30 Un procedimiento para la preparacion de n- (4- (beta-fenoxiacetamidoetil) -bencenosulfonil) -n'-ciclohexilurea Expired ES312479A1 (es)

Applications Claiming Priority (1)

Application Number	Priority Date	Filing Date	Title
DE312479X		1963-10-19

Publications (1)

Publication Number	Publication Date
ES312479A1 true ES312479A1 (es)	1966-04-01

Family

ID=38571774

Family Applications (1)

Application Number	Title	Priority Date	Filing Date
ES0312479A Expired ES312479A1 (es)	1963-10-19	1965-04-30	Un procedimiento para la preparacion de n- (4- (beta-fenoxiacetamidoetil) -bencenosulfonil) -n'-ciclohexilurea

Country Status (1)

Country	Link
ES (1)	ES312479A1 (es)

1965
- 1965-04-30 ES ES0312479A patent/ES312479A1/es not_active Expired

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