Ammonia → Ethyl 4-isopropylthiazole-2-carboxylate

HRID 420032Notes

Reaction equation

HRID 420032 reaction equation
Br[CH2:2][C:3](=O)[CH:4]([CH3:6])[CH3:5].C(OC(C1O[S:15]C=CC=1)=O)C.[NH3:19].[CH3:20][CH2:21][O:22][C:23]([CH3:25])=[O:24]>C(O)C.O>[CH:4]([C:3]1[N:19]=[C:25]([C:23]([O:22][CH2:21][CH3:20])=[O:24])[S:15][CH:2]=1)([CH3:6])[CH3:5]

Participants

7

Reactant 4

HCID 222AmmoniaHCID 8857Ethyl AcetateHCID 108990371-Bromo-3-methylbutan-2-oneHCID 86627749Ethylthioxamate

Product 1

HCID 10821861Ethyl 4-isopropylthiazole-2-carboxylate

Reagents, catalysts & solvents 2

HCID 702EthanolSolventHCID 962WaterSolvent

Conditions

Temperature
0 °C

Procedure

A solution of compound 35 (3.5 g, 1.25 eq.) and ethylthioxamate (2.3 g, 1 eq.) in ethanol (40 mL) was heated to 80° C. for 6 hrs, and then cooled to 0° C. The reaction mixture was diluted with water and EtOAc, and then neutralized to pH 7 with NH3 (28%). The aqueous layer was extracted with EtOAc. The combined organic layers were dried over sodium sulfate and then removed under reduced pressure. The residue was purified by chromatography on silica gel to yield compound 36 as yellow oil in quantitative yield.

Workup

  1. extractionThe aqueous layer was extracted with EtOAc
  2. dry with materialThe combined organic layers were dried over sodium sulfate
  3. customremoved under reduced pressure
  4. customThe residue was purified by chromatography on silica gel

Sources & evidence

ORD record
ord-adeacaea1c8c45a398b96c9838e645ac
Source dataset
uspto-grants-2012_01
Patent number
US08093379B2

Reaction notes

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