2-Aminothiazole → 4-Iodo-N-(thiazol-2-yl)benzenesulfonamide

HRID 1808252Notes

Reaction equation

HRID 1808252 reaction equation
[I:1][C:2]1[CH:7]=[CH:6][C:5]([S:8](Cl)(=[O:10])=[O:9])=[CH:4][CH:3]=1.[NH2:12][C:13]1[S:14][CH:15]=[CH:16][N:17]=1>N1C=CC=CC=1>[I:1][C:2]1[CH:7]=[CH:6][C:5]([S:8]([NH:12][C:13]2[S:14][CH:15]=[CH:16][N:17]=2)(=[O:10])=[O:9])=[CH:4][CH:3]=1

Participants

4

Reactant 2

HCID 21552-AminothiazoleHCID 73994-Iodobenzenesulfonyl chloride

Product 1

HCID 10193184-Iodo-N-(thiazol-2-yl)benzenesulfonamideYield 53.7%

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

4-Iodobenzenesulfonyl chloride (1.8 g, 6.0 mmol, 1.0 equiv) was added portion-wise to a 0° C. solution of 2-aminothiazole (654 mg, 6.53 mmol, 1.1 equiv) in 4.91 mL of anhydrous pyridine. After addition was complete, the reaction mixture was warmed to ambient temperature. After 3 d, the reaction mixture was concentrated in vacuo. The residue was treated with MeOH and ether to precipitate the product. The solid was collected by filtration, washing with ether, to afford the product as a light brown solid (1.18 g, 49%).

Workup

  1. additionAfter addition
  2. concentrationthe reaction mixture was concentrated in vacuo
  3. additionThe residue was treated with MeOH and ether
  4. customto precipitate the product
  5. filtrationThe solid was collected by filtration
  6. washwashing with ether

Sources & evidence

ORD record
ord-62c0879b7c7b4cbcb1792f130acba41e
Source dataset
uspto-grants-2013_01
Patent number
US08357711B2

Reaction notes

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