Pyridine → HCID 57743007, compound

HRID 2043591Notes

Reaction equation

HRID 2043591 reaction equation
[I:1][C:2]1[C:3]([CH3:8])=[N:4][NH:5][C:6]=1[CH3:7].[CH3:9][C:10]1[CH:15]=[CH:14][C:13]([S:16](Cl)(=[O:18])=[O:17])=[CH:12][CH:11]=1.N1C=CC=CC=1>C(Cl)Cl>[I:1][C:2]1[C:3]([CH3:8])=[N:4][N:5]([S:16]([C:13]2[CH:14]=[CH:15][C:10]([CH3:9])=[CH:11][CH:12]=2)(=[O:18])=[O:17])[C:6]=1[CH3:7]

Participants

5

Reactant 3

HCID 1049PyridineHCID 73974-Toluenesulfonyl chlorideHCID 971153,5-Dimethyl-4-iodo-1H-pyrazole

Product 1

HCID 57743007HCID 57743007, compoundYield 74%

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent

Procedure

In a 50 ml reaction vessel under argon, a solution of crude 4-iodo-3,5-dimethyl-1H-pyrazole x52 (1.15 g, 5.2 mmol) in 25 ml of dry CH2Cl2 is added to 4-methylbenzenesulfonyl chloride (1.18 g, 6.2 mmol). Pyridine (0.42 ml, 5.2 mmol) is added and the mixture is stirred for 16 h at room temperature. The organic phase is washed with water, dried over MgSO4, filtered and concentrated. The residue is purified by column chromatography on silicagel (CH2Cl2/hexane: 70/30 (v/v)) to afford 4-iodo-3,5-dimethyl-1-[(4-methylphenyl)sulfonyl]-1H-pyrazole x53 (1.44 g).

Workup

  1. customIn a 50 ml reaction vessel under argon
  2. washThe organic phase is washed with water
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe residue is purified by column chromatography on silicagel (CH2Cl2/hexane: 70/30 (v/v))

Sources & evidence

ORD record
ord-78460f9a0d95495aa08bb8dd85d56f4a
Source dataset
uspto-grants-2013_11
Patent number
US08586623B2

Reaction notes

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