m-Chloroperbenzoic acid → HCID 15676629, compound

HRID 1974455Notes

Reaction equation

HRID 1974455 reaction equation
ClC1C=C(C=CC=1)C(OO)=[O:6].[CH:12]([C:15]1([CH3:39])[C:19](=[O:20])[NH:18][C:17]([C:21]2[N:30]=[CH:29][C:28]([CH2:31][S:32][C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)=[CH:27][C:22]=2[C:23]([O:25][CH3:26])=[O:24])=[N:16]1)([CH3:14])[CH3:13].C(=O)(O)[O-].[Na+]>C(Cl)Cl.S(S([O-])=O)([O-])(=O)=O.[Na+].[Na+]>[CH:12]([C:15]1([CH3:39])[C:19](=[O:20])[NH:18][C:17]([C:21]2[N:30]=[CH:29][C:28]([CH2:31][S:32]([C:33]3[CH:38]=[CH:37][CH:36]=[CH:35][CH:34]=3)=[O:6])=[CH:27][C:22]=2[C:23]([O:25][CH3:26])=[O:24])=[N:16]1)([CH3:14])[CH3:13]

Participants

6

Reactant 3

HCID 70297m-Chloroperbenzoic acidHCID 516892Sodium BicarbonateHCID 15676628HCID 15676628, compound

Product 1

HCID 15676629HCID 15676629, compoundYield 93.1%

Reagents, catalysts & solvents 2

HCID 6344DichloromethaneSolventHCID 656671Sodium PyrosulfiteSolvent

Conditions

Temperature
-78 °C

Procedure

3-Chloroperoxybenzoic acid (20 mL, 0.00252 mol) is added dropwise to a -78° C. solution of 2-(4-isopropyl-4-methyl-5-oxo-2-imidazolin-2-yl)-5-[(phenylthio)methyl]nicotinic acid, methyl ester (1.0 g, 0.00252 mol) and sodium bicarbonate (0.2 g, 0.00238 mol) in methylene chloride. The reaction mixture is stirred at -78° C. for 30 minutes and then at room temperature for 24 hours. The reaction mixture is diluted with 5% sodium metabisulfite solution. The methylene chloride layer is separated, washed with saturated sodium bicarbonate solution, dried over anhydrous magnesium sulfate and concentrated in vacuo to yield a yellow oil. The oil is chromatographed using silica gel and hexanes/ethyl acetate (1:1) to (1:2) to (1:9) and finally 100% ethyl acetate as eluant to give the title compound as a yellow solid (0.97 g, 90%), mp 132°-136° C., identified by IR and NMR spectral analyses.

Workup

  1. waitat room temperature for 24 hours
  2. customThe methylene chloride layer is separated
  3. washwashed with saturated sodium bicarbonate solution
  4. dry with materialdried over anhydrous magnesium sulfate
  5. concentrationconcentrated in vacuo
  6. customto yield a yellow oil
  7. customThe oil is chromatographed

Sources & evidence

ORD record
ord-8c3a9dd8b2f64039a10ed2e95928c7c6
Source dataset
uspto-grants-1994_02
Patent number
US05283230

Reaction notes

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