Pyridine → N-{2-[N-(5-chloro(2-pyridyl))carbamoyl](3-thienyl)}(4-(2-sulfamoylphenyl)phenyl]carboxamide

HRID 12145Notes

Reaction equation

HRID 12145 reaction equation
C([NH:5][S:6]([C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][C:10]=1[C:15]1[CH:23]=[CH:22][C:18]([C:19](Cl)=[O:20])=[CH:17][CH:16]=1)(=[O:8])=[O:7])(C)(C)C.[NH2:24][C:25]1[CH:29]=[CH:28][S:27][C:26]=1[C:30]([NH:32][C:33]1[CH:38]=[C:37](Cl)[CH:36]=[CH:35][N:34]=1)=[O:31].N1C=CC=CC=1.[Cl:46]CCl>>[Cl:46][C:36]1[CH:37]=[CH:38][C:33]([NH:32][C:30]([C:26]2[S:27][CH:28]=[CH:29][C:25]=2[NH:24][C:19]([C:18]2[CH:17]=[CH:16][C:15]([C:10]3[CH:11]=[CH:12][CH:13]=[CH:14][C:9]=3[S:6](=[O:7])(=[O:8])[NH2:5])=[CH:23][CH:22]=2)=[O:20])=[O:31])=[N:34][CH:35]=1

Participants

5

Reactant 4

HCID 1049PyridineHCID 6344Dichloromethane2×HCID 22596369HCID 22596369, compoundHCID 226016743-Amino-2-(4-chloro-2-pyridinyl)aminocarbonyl thiophene

Product 1

HCID 10229449N-{2-[N-(5-chloro(2-pyridyl))carbamoyl](3-thienyl)}(4-(2-sulfamoylphenyl)phenyl]carboxamide

Procedure

A solution of 4-(2-{[(tert-butyl)amino]sulfonyl}phenyl)benzoyl chloride (1 equiv), 3-amino-2-(4-chloro-2-pyridinyl)aminocarbonyl thiophene (1 equiv), pyridine (5 equiv) in dichloromethane was stirred at rt overnight. The mixture was diluted with dichloromethane, washed with water, dried over Na2SO4, filtered and evaporated. The residue was refluxed with 1 mL of TFA for 2 h. After evaporation, reverse phase HPLC gave the title product. ES-MS 513(M+1).

Workup

  1. washwashed with water
  2. dry with materialdried over Na2SO4
  3. filtrationfiltered
  4. customevaporated
  5. temperatureThe residue was refluxed with 1 mL of TFA for 2 h
  6. customAfter evaporation

Sources & evidence

ORD record
ord-c06c18e12e844b22ab1552843c34d3b0
Source dataset
uspto-grants-2010_06
Patent number
US07727982B2

Reaction notes

Loading…