Hydrochloric Acid → HCID 15729161, compound
Reaction equation
C([NH:4][C:5]1[S:6][C:7]([S:10][C:11]2[N:12]([CH3:16])[CH:13]=[CH:14][N:15]=2)=[CH:8][N:9]=1)(=O)C.Cl>C(O)(=O)C>[NH2:4][C:5]1[S:6][C:7]([S:10][C:11]2[N:12]([CH3:16])[CH:13]=[CH:14][N:15]=2)=[CH:8][N:9]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A solution of 2-acetylamino-5-(1-methylimidazol-2-ylthio)thiazole (7.0 g) in a mixture of acetic acid (100 ml) and aqueous 6N-hydrochloric acid (20 ml) was refluxed for 3.5 hours with stirring. The reaction mixture was concentrated under reduced pressure and the residue was adjusted to pH 8 using aqueous sodium bicarbonate under ice cooling. The precipitates were collected by filtration, washed with water and dried in vacuo to give 2-amino-5-(1-methylimidazol-2-ylthio)thiazole (4.9 g, yield: 83.9%). mp: 180°-190° C. (dec.) IR (Nujol): 3300, 3150, 1620, 1530, 1280, 1220 cm-1
Workup
- temperaturewas refluxed for 3.5 hours
- concentrationThe reaction mixture was concentrated under reduced pressure
- filtrationThe precipitates were collected by filtration
- washwashed with water
- customdried in vacuo
Sources & evidence
- ORD record
- ord-5fa7ea58a6104b1ca3d449fa43df4c35
- Source dataset
- uspto-grants-1993_10
- Patent number
- US05256675
Reaction notes
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