Sodium Hydroxide → HCID 178429605, compound

HRID 2077009Notes

Reaction equation

HRID 2077009 reaction equation
C([NH:9][C:10](=[O:27])[NH:11][C:12]1[S:16][C:15]([C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])=[C:14]([CH3:24])[C:13]=1[C:25]#[N:26])(=O)C1C=CC=CC=1.[OH-].[Na+]>CCO>[NH2:26][C:25]1[C:13]2[C:14]([CH3:24])=[C:15]([C:17]([O:19][C:20]([CH3:23])([CH3:22])[CH3:21])=[O:18])[S:16][C:12]=2[NH:11][C:10](=[O:27])[N:9]=1

Participants

4

Reactant 2

HCID 14798Sodium HydroxideHCID 57456933Tert-butyl 5-(3-benzoylureido)-4-cyano-3-methylthiophene-2-carboxylate

Product 1

HCID 178429605HCID 178429605, compoundYield 63%

Reagents, catalysts & solvents 1

HCID 702EthanolSolvent

Procedure

To a suspension of tert-butyl 5-(3-benzoylureido)-4-cyano-3-methylthiophene-2-carboxylate (example 64a) (18 g, 60.52 mmol) in EtOH (200 mL) was added NaOH (75 mL, 2N). The suspension became clear, and the mixture was heated to reflux for 30 min. After cooling to rt, the reaction was filtered, and the filtrate was cooled to 0° C. in an ice/water bath. The solution was neutralized with 10% acetic acid. The precipitated solid was collected by filtration, and heated in EtOH at 80° C. under N2 for 20 min. After cooling to rt, the product was collected by filtration and washed with 10% EtOH in H2O to yield tert-Butyl 4-amino-5-methyl-2-oxo-1,2-dihydrothieno[2,3-d]pyrimidine-6-carboxylate (10.73 g, 63%) as a brown solid. 1H NMR (400 MHz, DMSO-d6) δ 1.51 (s, 9H), 2.73 (s, 3H), 3.18 (s, 2H). MS 282.2 (MH+).

Workup

  1. temperaturethe mixture was heated
  2. temperatureto reflux for 30 min
  3. filtrationthe reaction was filtered
  4. temperaturethe filtrate was cooled to 0° C. in an ice/water bath
  5. filtrationThe precipitated solid was collected by filtration
  6. temperatureheated in EtOH at 80° C. under N2 for 20 min
  7. temperatureAfter cooling to rt
  8. filtrationthe product was collected by filtration
  9. washwashed with 10% EtOH in H2O

Sources & evidence

ORD record
ord-e5d2412dcd1f419d89a8aa01623c8cc3
Source dataset
uspto-grants-2011_04
Patent number
US07928111B2

Reaction notes

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