Water → HCID 69338013, compound

HRID 2086191Notes

Reaction equation

HRID 2086191 reaction equation
[C:1]([O:4][CH2:5][C@H:6]([CH3:18])[CH2:7][CH:8]([NH:14][C:15](=[O:17])[CH3:16])[C:9]1[S:10][CH:11]=[CH:12][CH:13]=1)(=[O:3])[CH3:2].[Br:19]N1C(=O)CCC1=O.O>CN(C)C=O>[C:1]([O:4][CH2:5][C@H:6]([CH3:18])[CH2:7][CH:8]([NH:14][C:15](=[O:17])[CH3:16])[C:9]1[S:10][C:11]([Br:19])=[CH:12][CH:13]=1)(=[O:3])[CH3:2]

Participants

5

Procedure

(2R)-Acetylamino-2-methyl-4-(thiophen-2-yl)butyl acetate (1.81 g, 6.70 mmol) obtained in Example 47(b) was dissolved in dimethylformamide (20 ml), and N-bromosuccinimide (1.27 g, 7.11 mmol) was added thereto in an ice bath followed by stirring under a nitrogen atmosphere for 10 minutes in an ice bath and then overnight at room temperature. The reaction solution was poured into water, extracted with ethyl acetate, and the ethyl acetate layer was washed with a saturated aqueous sodium chloride solution The ethyl acetate layer was dried over anhydrous sodium sulfate, and the solvent was evaporated in vacuo. The residue was purified by chromatography on a silica gel column (elution solvent; hexane:ethyl acetate=3:1-1:2) to afford the title compound (2.32 g, 99% yield).

Workup

  1. customin an ice bath followed
  2. customovernight
  3. customat room temperature
  4. extractionextracted with ethyl acetate
  5. washthe ethyl acetate layer was washed with a saturated aqueous sodium chloride solution The ethyl acetate layer
  6. dry with materialwas dried over anhydrous sodium sulfate
  7. customthe solvent was evaporated in vacuo
  8. customThe residue was purified by chromatography on a silica gel column (elution solvent; hexane:ethyl acetate=3:1-1:2)

Sources & evidence

ORD record
ord-912fb6102291476681693df3004c1c84
Source dataset
uspto-grants-2004_04
Patent number
US06723745B2

Reaction notes

Loading…