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Urea → Ethyl 2-amino-4-(trifluoromethyl)-1,3-oxazole-5-carboxylate

HRID 1020337
Notes
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Reaction equation

HRID 1020337 reaction equation
[NH2:1][C:2]([NH2:4])=[O:3].[F:5][C:6]([F:17])([F:16])[C:7](=O)[CH:8](Cl)[C:9]([O:11][CH2:12][CH3:13])=[O:10]>CN(C=O)C.O>[NH2:1][C:2]1[O:3][C:8]([C:9]([O:11][CH2:12][CH3:13])=[O:10])=[C:7]([C:6]([F:5])([F:17])[F:16])[N:4]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

5

Reactant 2

HCID 1176UreaHCID 2737165Ethyl 2-chloro-4,4,4-trifluoro-3-oxobutanoate

Product 1

HCID 21850563Ethyl 2-amino-4-(trifluoromethyl)-1,3-oxazole-5-carboxylateYield 74%

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 6228DimethylformamideSolvent

Conditions

Temperature
120 °C

Procedure

To a suspension of urea (13.5 g) in DMF (50 mL) was added ethyl 4,4,4-trifluoro-2-chloroacetoacetate (10 mL) and the resulting reaction mixture was heated at 120° C. for 3 days. Then, the reaction mixture was cooled to RT and diluted with H2O (100 mL). Then, the reaction mixture was stirred at 0° C. for 1 h. The resulting precipitate was filtered, washed with H2O and dried in vacuo to yield ethyl 2-amino-4-trifluoromethyloxazole-5-carboxylate (A-1) as a white powder (9.8 g, 74% yield). LCMS (ESI) calcd for [M+1]+ 225.1. found 225.1.

Workup

  1. customthe resulting reaction mixture
  2. temperatureThen, the reaction mixture was cooled to RT
  3. filtrationThe resulting precipitate was filtered
  4. washwashed with H2O
  5. customdried in vacuo

Sources & evidence

ORD record
ord-6e5c2e472c064db1a58c107bd547b752
Source dataset
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US08716312B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes