Reaction #2483276

ord-60aab3a6b4de4566aab44bbf2a55fb9b

Reaction equation

CCCCCCCCCCCCn1nnc(NC(=O)CS(=O)(=O)Nc2c(C(C)C)cccc2C(C)C)n1
title compound
CCCCCCCCCCCCn1nnc(NC(=O)CS(=O)(=O)Nc2c(C(C)C)cccc2C(C)C)n1
2-(2,6-Diisopropyl-phenylsulfamoyl)-N-(dodecyl-2-H-tetrazol-5-yl)-acetamide
CCCCCCCCNCCCCCCCC
N,N-dioctylamine
→
CCCCCCCCN(CCCCCCCC)C(=O)CS(=O)(=O)Nc1c(C(C)C)cccc1C(C)C
2-(2,6-Diisopropylphenylsulfamoyl)-N,N-dioctylacetamide

Reactants

CCCCCCCCCCCCn1nnc(NC(=O)CS(=O)(=O)Nc2c(C(C)C)cccc2C(C)C)n1
title compound
CCCCCCCCCCCCn1nnc(NC(=O)CS(=O)(=O)Nc2c(C(C)C)cccc2C(C)C)n1
2-(2,6-Diisopropyl-phenylsulfamoyl)-N-(dodecyl-2-H-tetrazol-5-yl)-acetamide
CCCCCCCCNCCCCCCCC
N,N-dioctylamine

Reagents

None

Conditions

Detailed conditions
See reaction.notes.procedure_details.

Procedure

This compound was prepared in the same manner as for the title compound of Example 2, except that 2-DAT was replaced with N,N-dioctylamine, mp 107°-109° C.

Source

DOI: 10.6084/m9.figshare.5104873.v1Patent: US05491170uspto-grants-1996_02