ES312471A1 - Procedimiento para la preparacion de n-4-(beta-benzamidoetil) -bencenosulfonil n'-ciclohexilurea - Google Patents

Info

Publication number

ES312471A1

ES312471A1 ES0312471A ES312471A ES312471A1 ES 312471 A1 ES312471 A1 ES 312471A1 ES 0312471 A ES0312471 A ES 0312471A ES 312471 A ES312471 A ES 312471A ES 312471 A1 ES312471 A1 ES 312471A1

Authority

ES

Spain

Prior art keywords

beta

ethyl

benzamido

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

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• -1 beta-benzamidoethyl Chemical group 0.000 title abstract 6
• 238000000034 method Methods 0.000 title abstract 3
• 150000003839 salts Chemical class 0.000 abstract 4
• 239000002253 acid Substances 0.000 abstract 3
• HVFINYFNKGQDIY-UHFFFAOYSA-N [4-(2-benzamidoethyl)phenyl]sulfonylcarbamic acid Chemical compound C1=CC(S(=O)(=O)NC(=O)O)=CC=C1CCNC(=O)C1=CC=CC=C1 HVFINYFNKGQDIY-UHFFFAOYSA-N 0.000 abstract 2
• 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
• 150000002170 ethers Chemical class 0.000 abstract 2
• 125000003170 phenylsulfonyl group Chemical group C1(=CC=CC=C1)S(=O)(=O)* 0.000 abstract 2
• HUTMXFCLIJPFRE-UHFFFAOYSA-N 4-(2-benzamidoethyl)benzenesulfonyl chloride Chemical compound C1=CC(S(=O)(=O)Cl)=CC=C1CCNC(=O)C1=CC=CC=C1 HUTMXFCLIJPFRE-UHFFFAOYSA-N 0.000 abstract 1
• LLZAMKKHDGOYGH-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)N(C(=O)NC1CCCCC1)S(=O)(=O)C1=CC=C(C=C1)CCN Chemical compound C(C1=CC=CC=C1)(=O)N(C(=O)NC1CCCCC1)S(=O)(=O)C1=CC=C(C=C1)CCN LLZAMKKHDGOYGH-UHFFFAOYSA-N 0.000 abstract 1
• SFLQDIMKQJVBIH-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)NCCC1=CC=C(C=C1)S(=O)(=O)N=C=O Chemical compound C(C1=CC=CC=C1)(=O)NCCC1=CC=C(C=C1)S(=O)(=O)N=C=O SFLQDIMKQJVBIH-UHFFFAOYSA-N 0.000 abstract 1
• KUZYXAIASYDJRG-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)NCCC1=CC=C(C=C1)S(=O)(=O)NC(=S)NC1CCCCC1 Chemical compound C(C1=CC=CC=C1)(=O)NCCC1=CC=C(C=C1)S(=O)(=O)NC(=S)NC1CCCCC1 KUZYXAIASYDJRG-UHFFFAOYSA-N 0.000 abstract 1
• JVGTUAQOPLRVRJ-UHFFFAOYSA-N C(C1=CC=CC=C1)(=O)NCCC1=CC=C(C=C1)SNC(=O)NC1CCCCC1 Chemical compound C(C1=CC=CC=C1)(=O)NCCC1=CC=C(C=C1)SNC(=O)NC1CCCCC1 JVGTUAQOPLRVRJ-UHFFFAOYSA-N 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
• 239000004202 carbamide Substances 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
• 125000004430 oxygen atom Chemical group O* 0.000 abstract 1
• 229910052717 sulfur Inorganic materials 0.000 abstract 1
• 125000004434 sulfur atom Chemical group 0.000 abstract 1