Bromoacetic Acid → HCID 21298296, compound
Reaction equation
[C:1]([NH:4][C:5]1[S:9][C:8]([SH:10])=[N:7][CH:6]=1)(=[O:3])[CH3:2].Br[CH2:12][C:13]([OH:15])=[O:14]>CN(C=O)C>[C:1]([NH:4][C:5]1[S:9][C:8]([S:10][CH2:12][C:13]([OH:15])=[O:14])=[N:7][CH:6]=1)(=[O:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
3.48 g (20 mmol) of 5-acetamido-2-mercapto-1,3-thiazole were dissolved in 90 ml of dry DMF, 2.78 g (20 mmol) of bromoacetic acid were added, and the mixture was stirred at room temperature for 2 hours. The solvent was then removed in vacuo, and the solid residue was washed with diethyl ether. After recrystallization from isopropanol/diethyl ether, 3.1 g (67%) of the title compound were obtained.
Workup
- customThe solvent was then removed in vacuo
- washthe solid residue was washed with diethyl ether
- customAfter recrystallization from isopropanol/diethyl ether
Sources & evidence
- ORD record
- ord-f59bb8b3a7974d5f8e86eb075a8f8b98
- Source dataset
- uspto-grants-1988_08
- Patent number
- US04762848
Reaction notes
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