Potassium Hydroxide → HCID 178432820, compound

HRID 1825401Notes

Reaction equation

HRID 1825401 reaction equation
[OH-].[K+].[CH:3]1([O:8][C:9]2[C:10]([CH3:19])=[N:11][CH:12]=[C:13]([CH:18]=2)[C:14]([O:16]C)=[S:15])[CH2:7][CH2:6][CH2:5][CH2:4]1>O.CO>[CH:3]1([O:8][C:9]2[C:10]([CH3:19])=[N:11][CH:12]=[C:13]([CH:18]=2)[C:14]([OH:16])=[S:15])[CH2:4][CH2:5][CH2:6][CH2:7]1

Participants

5

Procedure

A solution of potassium hydroxide (582 mg) in water (6 mL) is added to a stirred solution of methyl 5-cyclopentyloxy-6methylthionicotinoate (920 mg) in methanol at room temperature and the mixture stirred for 6 hours. After concentrating in vacuo the mixture is diluted with water and acidified to pH 1 with aqueous 2 M hydrochloric acid. The product is extracted into ethyl acetate, the extracts treated with decolourising charcoal, dried (MgSO4) and evaporated. The residue is triturated with n-pentane to give 5-cyclopentyloxy-6-methylthionicotinic acid (640 mg) as a white solid, m.p. 177–8° C. [Elemental analysis:—C, 56.90; H, 6.02; N, 5.52%. calculated:—C, 56.90; H, 5.97; N, 5.53%.].

Workup

  1. concentrationAfter concentrating in vacuo the mixture
  2. additionis diluted with water
  3. extractionThe product is extracted into ethyl acetate
  4. additionthe extracts treated with decolourising charcoal
  5. dry with materialdried (MgSO4)
  6. customevaporated
  7. customThe residue is triturated with n-pentane

Sources & evidence

ORD record
ord-da81bb6808114245ae05eec21373052b
Source dataset
uspto-grants-2006_05
Patent number
US07045660B2

Reaction notes

Loading…