Water → HCID 66591349, compound

HRID 1092266Notes

Reaction equation

HRID 1092266 reaction equation
[OH-].[Na+].[CH3:3][N:4]([CH2:14][C:15]1[S:19][CH:18]=[C:17]([C:20]2[CH:25]=[CH:24][C:23]([CH:26]=[CH:27][C:28]([O:30]CC)=[O:29])=[CH:22][CH:21]=2)[CH:16]=1)[C:5](=[O:13])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12].O1CCCC1.CO.O>C(O)(=O)C>[CH3:3][N:4]([CH2:14][C:15]1[S:19][CH:18]=[C:17]([C:20]2[CH:21]=[CH:22][C:23]([CH:26]=[CH:27][C:28]([OH:30])=[O:29])=[CH:24][CH:25]=2)[CH:16]=1)[C:5](=[O:13])[CH2:6][CH2:7][CH2:8][CH2:9][CH2:10][CH2:11][CH3:12]

Participants

6

Reactant 4

HCID 962WaterHCID 14798Sodium HydroxideHCID 21899815MeOH tetrahydrofuranHCID 66591532HCID 66591532, compound

Product 1

HCID 66591349HCID 66591349, compoundYield 35%

Reagents, catalysts & solvents 1

HCID 176Acetic AcidSolvent

Procedure

230 mg (5.8 mmol, 10 eq) of sodium hydroxide are added to a solution of 250 mg (0.58 mmol, 1 eq) of ethyl 3-(4-{5-[(methyloctanoylamino)methyl]thiophen-3-yl}phenyl)acrylate in 4 mL of 9/1 tetrahydrofuran/methanol. The reaction mixture is stirred for 2 hours at room temperature. The reaction is stopped by adding 20 mL of water and 3 mL of acetic acid and is then extracted with ethyl acetate. The organic phases are combined and dried over sodium sulfate. The solvents are evaporated off and the residue is then chromatographed on silica gel (90/10 dichloromethane/methanol). The oil obtained is crystallized from pentane. 80 mg of 3-(4-{5-[(methyloctanoylamino)methyl]thiophen-3-yl}phenyl)acrylic acid are obtained. Yield=35%. m.p.=175° C.

Workup

  1. extractionis then extracted with ethyl acetate
  2. dry with materialdried over sodium sulfate
  3. customThe solvents are evaporated off
  4. customthe residue is then chromatographed on silica gel (90/10 dichloromethane/methanol)
  5. customThe oil obtained
  6. customis crystallized from pentane

Sources & evidence

ORD record
ord-06932f773b224f53aafda707d27cf1b9
Source dataset
uspto-grants-2012_03
Patent number
US08129416B2

Reaction notes

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