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Benzenesulfonamide → 4-[13-(4-chlorophenyl)tridec-12-ynylamino]-N-(phenylsulfonyl)benzamide

HRID 2057670
ノート
印刷プレビュー

反応式

HRID 2057670 の反応式
[C:1]1([S:7]([NH2:10])(=[O:9])=[O:8])[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[H-].[Na+].[Cl:13][C:14]1[CH:19]=[CH:18][C:17]([C:20]#[C:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][NH:33][C:34]2[CH:42]=[CH:41][C:37]([C:38](O)=[O:39])=[CH:36][CH:35]=2)=[CH:16][CH:15]=1.S(Cl)(Cl)=O>C(COC)OC.C(Cl)Cl.CC(N(C)C)=O>[Cl:13][C:14]1[CH:15]=[CH:16][C:17]([C:20]#[C:21][CH2:22][CH2:23][CH2:24][CH2:25][CH2:26][CH2:27][CH2:28][CH2:29][CH2:30][CH2:31][CH2:32][NH:33][C:34]2[CH:35]=[CH:36][C:37]([C:38]([NH:10][S:7]([C:1]3[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=3)(=[O:9])=[O:8])=[O:39])=[CH:41][CH:42]=2)=[CH:18][CH:19]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

8

反応物 4

HCID 7370BenzenesulfonamideHCID 24386Thionyl ChlorideHCID 24758Sodium hydrideHCID 203309694-[13-(4-Chlorophenyl)-12-tridecynylamino]benzoic acid

生成物 1

HCID 203312704-[13-(4-chlorophenyl)tridec-12-ynylamino]-N-(phenylsulfonyl)benzamide

試薬・触媒・溶媒 3

HCID 6344
Dichloromethane
溶媒
HCID 80711,2-Dimethoxyethane溶媒
HCID 31374Dimethylacetamide溶媒2 回

実験手順

A solution of 31.4 g. of benzenesulfonamide in 250 ml. of dry dimethylacetamide is added dropwise, with stirring and cooling, to a suspension of 5.5 g. of sodium hydride in 100 ml. of dry dimethylacetamide during 30 minutes at room temperature. Stirring is continued for a further 30 minutes. In the meantime, a mixture of 36.5 g. of 4-[13-(4-chlorophenyl)tridec-12-ynylamino]benzoic acid in 100 ml. of methylene chloride, 300 ml. of dimethoxyethane, and 40 ml. of thionyl chloride is refluxed for 1 hour and 15 minutes. The solution is evaporated and to the resulting oil residue is added, in one portion, the previously prepared mixture of sodium benzenesulfonamide in dimethylacetamide. The mixture is stirred for 30 minutes, without cooling, and then filtered. The filtrate is poured into 2 l. of water and 250 ml. of saturated sodium chloride solution. The product is collected by filtration and then dissolved in methylene chloride, the mixture is filtered through diatomaceous earth, and brine is added to break the emulsion. The layers are separated, the organic phase is dried and evaporated. The residue is crystallized from toluene to yield 4-[13-(4-chlorophenyl)tridec-12-ynylamino]-N-(phenylsulfonyl)benzamide.

後処理

  1. temperaturecooling, to a suspension of 5.5 g
  2. stirringStirring
  3. additionIn the meantime, a mixture of 36.5 g
  4. customThe solution is evaporated and to the resulting oil residue
  5. additionis added, in one portion
  6. additionthe previously prepared mixture of sodium benzenesulfonamide in dimethylacetamide
  7. stirringThe mixture is stirred for 30 minutes
  8. temperaturewithout cooling
  9. filtrationfiltered
  10. additionThe filtrate is poured into 2 l
  11. filtrationThe product is collected by filtration
  12. dissolutiondissolved in methylene chloride
  13. filtrationthe mixture is filtered through diatomaceous earth, and brine
  14. additionis added
  15. customThe layers are separated
  16. customthe organic phase is dried
  17. customevaporated
  18. customThe residue is crystallized from toluene

出典と根拠

ORDレコード
ord-28966f082ad1490e8f2521413ef3e960
出典データセット
uspto-grants-1980_07
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US04211783

反応ノート

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