Sodium Hydroxide → α-(1,1-Dimethylethoxy)-5,6,7,8-tetrahydro-2-methyl-4-(6-methyl-3-pyridinyl)[1]benzothieno[2,3-b]pyridine-3-acetic acid

HRID 1627912Notes

Reaction equation

HRID 1627912 reaction equation
[CH3:1][C:2]1[N:7]=[C:6]2[S:8][C:9]3[CH2:14][CH2:13][CH2:12][CH2:11][C:10]=3[C:5]2=[C:4]([C:15]2[CH:16]=[N:17][C:18]([CH3:21])=[CH:19][CH:20]=2)[C:3]=1[CH:22]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])[C:23]([O:25]C)=[O:24].[OH-].[Na+]>CO>[CH3:1][C:2]1[N:7]=[C:6]2[S:8][C:9]3[CH2:14][CH2:13][CH2:12][CH2:11][C:10]=3[C:5]2=[C:4]([C:15]2[CH:16]=[N:17][C:18]([CH3:21])=[CH:19][CH:20]=2)[C:3]=1[CH:22]([O:27][C:28]([CH3:31])([CH3:30])[CH3:29])[C:23]([OH:25])=[O:24]

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 49806580HCID 49806580, compound

Product 1

HCID 49806338α-(1,1-Dimethylethoxy)-5,6,7,8-tetrahydro-2-methyl-4-(6-methyl-3-pyridinyl)[1]benzothieno[2,3-b]pyridine-3-acetic acidYield 20.6%

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
60 °C

Procedure

To a solution of methyl 2-[2-methyl-4-(6-methylpyridin-3-yl)-5,6,7,8-tetrahydro[1]benzothieno[2,3-b]pyridin-3-yl]-2-tert-butoxyacetate (0.035 g; 0.080 mmol) in methanol (1 mL) was added a solution of sodium hydroxide 10 N (0.100 mL; 1 mmol) and the mixture was heated at 60° C. for 18 h. The volatiles were removed under reduced pressure and the residue was dissolved in water. The mixture was then acidified by adding 1N HCl until a precipitate was formed. The solid was filtered, washed with water and dried under reduced pressure. The crude product was suspended in a mixture of acetonitrile and methanol, filtered, washed with acetonitrile and dried under reduced pressure to furnish 0.007 g (20%) of the title compound as a white solid.

Workup

  1. customThe volatiles were removed under reduced pressure
  2. dissolutionthe residue was dissolved in water
  3. additionby adding 1N HCl until a precipitate
  4. customwas formed
  5. filtrationThe solid was filtered
  6. washwashed with water
  7. customdried under reduced pressure
  8. additionThe crude product was suspended in a mixture of acetonitrile and methanol
  9. filtrationfiltered
  10. washwashed with acetonitrile
  11. customdried under reduced pressure

Sources & evidence

ORD record
ord-2967ce1db89a4d9088478e1c74c069ae
Source dataset
uspto-grants-2014_07
Patent number
US08785638B2

Reaction notes

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