Trifluoroacetic acid → Ethyl[7-(methyloxy)-3-oxo-6-(trifluoromethyl)-2,3-dihydro-4H-1,4-benzoxazin-4-yl]acetate

HRID 2114398Notes

Reaction equation

HRID 2114398 reaction equation
[CH3:1][O:2][C:3]1[C:13]([C:14]([F:17])([F:16])[F:15])=[CH:12][C:6]2[NH:7][C:8](=[O:11])[CH2:9][O:10][C:5]=2[CH:4]=1.[H-].[Na+].Br[CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23].FC(F)(F)C(O)=O>O1CCCC1.CC#N.O>[CH3:1][O:2][C:3]1[C:13]([C:14]([F:17])([F:15])[F:16])=[CH:12][C:6]2[N:7]([CH2:21][C:22]([O:24][CH2:25][CH3:26])=[O:23])[C:8](=[O:11])[CH2:9][O:10][C:5]=2[CH:4]=1

Participants

7

Reactant 4

HCID 6422Trifluoroacetic acidHCID 7748Ethyl bromoacetateHCID 24758Sodium hydrideHCID 575012767-(methyloxy)-6-(trifluoromethyl)-2H-1,4-benzoxazin-3(4H)-one

Product 1

HCID 57437814Ethyl[7-(methyloxy)-3-oxo-6-(trifluoromethyl)-2,3-dihydro-4H-1,4-benzoxazin-4-yl]acetateYield 69%

Reagents, catalysts & solvents 2

HCID 8028TetrahydrofuranSolvent2×HCID 18373917Acetonitrile--water (1/1)Solvent

Procedure

A solution of 7-(methyloxy)-6-(trifluoromethyl)-2H-1,4-benzoxazin-3(4H)-one (0.39 g, 1.6 mmol) dissolved in 1 mL of anhydrous tetrahydrofuran was added drop-wise to a mixture of sodium hydride (60% by weight in mineral oil, 0.068 g, 1.7 mmol) suspended in 2 mL of anhydrous tetrahydrofuran under argon. The mixture was allowed to stir at room temperature for 10 minutes and then ethyl bromoacetate (0.21 mL, 1.9 mmol) was added to the mixture and stirred vigorously for 18 hours before it was determined to be complete by LCMS (two Aquasil C18, 20×1 mm columns were run in sequence, 4 minutes at 0.1 mL/min, 1-99% CH3CN/H2O with 0.018% trifluoroacetic acid, ES) Rt=2.0 min and m/e 334 [M+1]+. The reaction was quenched by adding 5 mL of a 4 M solution of hydrochloric acid in dioxane. After allowing the mixture to stir for one hour, all of the volatiles were removed by rotary evaporation, and the crude residue was purified by silica gel chromatography (40 g Redisep column, silica, 40 um, 60 Å, 35 mL/min, A: methylene chloride, B: methanol, B: 0% to 10% over 30 min; detection at 214 nm) to give ethyl [7-(methyloxy)-3-oxo-6-(trifluoromethyl)-2,3-dihydro-4H-1,4-benzoxazin-4-yl]acetate (0.36 g, 1.1 mmol, 69%) of an off-white amorphous solid. MS (ES) m/e 334 [M+1]+.

Workup

  1. additionwas added drop-wise
  2. stirringstirred vigorously for 18 hours before it
  3. customThe reaction was quenched
  4. additionby adding 5 mL of a 4 M solution of hydrochloric acid in dioxane
  5. stirringto stir for one hour
  6. customall of the volatiles were removed by rotary evaporation
  7. customthe crude residue was purified by silica gel chromatography (40 g Redisep column, silica, 40 um, 60 Å, 35 mL/min
  8. waitA: methylene chloride, B: methanol, B: 0% to 10% over 30 min

Sources & evidence

ORD record
ord-27a1c845480e4850a3632d47d38e8e47
Source dataset
uspto-grants-2008_10
Patent number
US07432258B2

Reaction notes

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