Potassium Hydroxide → 4-(4-Cyanophenyl)-6-methyl-2-(methylsulfanyl)-1-[3-(trifluoromethyl)phenyl]-1,4-dihydro-5-pyrimidinecarboxylic acid

HRID 1921142Notes

Reaction equation

HRID 1921142 reaction equation
[C:1]([C:3]1[CH:8]=[CH:7][C:6]([CH:9]2[C:14]([C:15]([O:17]C)=[O:16])=[C:13]([CH3:19])[N:12]([C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:28])[F:27])[CH:21]=3)[C:11]([S:30][CH3:31])=[N:10]2)=[CH:5][CH:4]=1)#[N:2].[OH-].[K+]>C1COCC1.C(O)C.O.O>[C:1]([C:3]1[CH:4]=[CH:5][C:6]([CH:9]2[C:14]([C:15]([OH:17])=[O:16])=[C:13]([CH3:19])[N:12]([C:20]3[CH:25]=[CH:24][CH:23]=[C:22]([C:26]([F:29])([F:28])[F:27])[CH:21]=3)[C:11]([S:30][CH3:31])=[N:10]2)=[CH:7][CH:8]=1)#[N:2]

Participants

5

Procedure

Methyl 4-(4-cyanophenyl)-6-methyl-2-(methylsulfanyl)-1-[3-(trifluoromethyl)-phenyl]-1,4-dihydro-5-pyrimidinecarboxylate Example 8; 9.51 g, 21.4 mmol) is dissolved in 175 ml THF/ethanol/water (10:5:1). Potassium hydroxide (3.59 g, 64.1 mmol) is added, and the reaction mixture is stirred overnight. The reaction mixture is diluted with 100 ml of water, and the aqueous phase is washed with diethyl ether. The resulting aqueous phase is acidified to pH 1 with hydrochloric acid, and the resulting precipitate is filtered off, dissolved in ethyl acetate and washed with water. After drying with sodium sulfate, the solvent is removed in vacuo to give the product.

Workup

  1. washthe aqueous phase is washed with diethyl ether
  2. filtrationthe resulting precipitate is filtered off
  3. dissolutiondissolved in ethyl acetate
  4. washwashed with water
  5. dry with materialAfter drying with sodium sulfate
  6. customthe solvent is removed in vacuo
  7. customto give the product

Sources & evidence

ORD record
ord-304cab3197154a5eb07125d5537e0080
Source dataset
uspto-grants-2012_05
Patent number
US08173665B2

Reaction notes

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