Sulfuric Acid → HCID 58537915, compound

HRID 2176832Notes

Reaction equation

HRID 2176832 reaction equation
[Cl:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([CH3:9])=[CH:4][C:3]=1[CH2:10][C:11]([N:13]([C:15]1([C:23]#N)[CH2:20][CH2:19][N:18]([O:21][CH3:22])[CH2:17][CH2:16]1)[CH3:14])=[O:12].S(=O)(=O)(O)[OH:26].[OH-].[Na+]>CO>[Cl:1][C:2]1[CH:7]=[C:6]([CH3:8])[C:5]([CH3:9])=[CH:4][C:3]=1[C:10]1[C:11](=[O:12])[N:13]([CH3:14])[C:15]2([CH2:20][CH2:19][N:18]([O:21][CH3:22])[CH2:17][CH2:16]2)[C:23]=1[OH:26]

Participants

5

Reactant 3

HCID 1118Sulfuric Acid3×HCID 14798Sodium HydroxideHCID 58537989HCID 58537989, compound

Product 1

HCID 58537915HCID 58537915, compoundYield 19.5%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Procedure

To a solution of 2-(2-chloro-4,5-dimethyl-phenyl)-N-(4-cyano-1-methoxy-piperidin-4-yl)-N-methyl-acetamide (compound P4.27) (1.15 g, 3.29 mmol) in methanol (˜3 ml) at 10° C. was added concentrated sulfuric acid (0.876 ml, 16.43 mmol) dropwise and the reaction mixture was stirred at room temperature overnight. After further treatment with concentrated sulfuric acid (0.876 ml, 16.43 mmol) and stirring at 80° C. overnight, additional concentrated sulfuric acid (0.876 ml, 16.43 mmol) was added and stirring continued at 90° C. over another night. The mixture was poured on ice, neutralised carefully with 30% aqueous sodium hydroxide to pH 5-6, the resulting precipitate filtered and dried to afford a first crop of product as a beige solid (225 mg). The mother liquor was concentrated, and the residue purified by chromatography on silica gel (ethyl acetate) to further deliver 462 mg of product as a yellowish solid. Yield: 687 mg of 3-(2-chloro-4,5-dimethyl-phenyl)-4-hydroxy-8-methoxy-1-methyl-1,8-diaza-spiro[4.5]dec-3-en-2-one (title compound P2.26) as a solid, mp 191-192° C.

Workup

  1. stirringstirring
  2. waitcontinued at 90° C. over another night
  3. filtrationthe resulting precipitate filtered
  4. customdried

Sources & evidence

ORD record
ord-18d734a3ef92441c9295093c86115265
Source dataset
uspto-grants-2015_06
Patent number
US09067892B2

Reaction notes

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