Methyl iodide → HCID 68680176, compound

HRID 2240054Notes

Reaction equation

HRID 2240054 reaction equation
[Cl:1][CH2:2][CH2:3][O:4][C:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:13]=1[NH:12][N:11]=[C:10]2[S:14]([C:17]1[C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH:20]=[CH:19][CH:18]=1)(=[O:16])=[O:15].CI.[C:29](=O)([O-])[O-].[K+].[K+]>CN(C=O)C.O>[Cl:1][CH2:2][CH2:3][O:4][C:5]1[CH:6]=[CH:7][CH:8]=[C:9]2[C:13]=1[N:12]([CH3:29])[N:11]=[C:10]2[S:14]([C:17]1[C:26]2[C:21](=[CH:22][CH:23]=[CH:24][CH:25]=2)[CH:20]=[CH:19][CH:18]=1)(=[O:16])=[O:15]

Participants

6

Reactant 3

HCID 6328Methyl iodideHCID 11430Potassium CarbonateHCID 178527287HCID 178527287, compound

Product 1

HCID 68680176HCID 68680176, compound

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228DimethylformamideSolvent

Procedure

A mixture of 7-(2-chloro-ethoxy)-3-(naphthalene-1-sulfonyl)-1-H-indazole (0.7 g, 1.8 mmoles), methyl iodide (0.28 mL, 2.17 mmoles), and potassium carbonate (0.29 g, 2.17 mmoles) in DMF (10 mL) was stirred together in a round bottom flask at room temperature for 2 hours. Reaction mixture was diluted with H2O, extracted with EtOAc, washed with water (2×), brine (1×), dried over Na2SO4, and concentrated under vacuum. The crude product was purified by HPLC using as eluent 30% EtOAc/hexane to afford the title compound as an off-white solid, 0.55 g, 1.375 mmoles.

Workup

  1. customReaction mixture
  2. extractionextracted with EtOAc
  3. washwashed with water (2×), brine (1×)
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated under vacuum
  6. customThe crude product was purified by HPLC

Sources & evidence

ORD record
ord-84ac7db8a4e94e568012028ff49b2493
Source dataset
uspto-grants-2010_05
Patent number
US07723329B2

Reaction notes

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