Hydrochloric Acid → HCID 18002792, compound
Reaction equation
[N:1]([CH2:4][C:5]([C:7]1[CH:16]=[CH:15][C:10]2[NH:11][C:12](=[O:14])[S:13][C:9]=2[CH:8]=1)=[O:6])=[N+]=[N-].[ClH:17]>CO.[Pd]>[ClH:17].[NH2:1][CH2:4][C:5]([C:7]1[CH:16]=[CH:15][C:10]2[NH:11][C:12](=[O:14])[S:13][C:9]=2[CH:8]=1)=[O:6]Participants
5
Reactant 2
Product 1
Reagents, catalysts & solvents 2
Procedure
6-(2-Azidoethanoyl)-3H-benzothiazol-2-one (0.5 g, 2.14 mmol) and Pd—C (5%, 0.17 g) in methanol (40 mL) and concentrated HCl (0.5 mL) were subjected to hydrogenation at 20 psi and 25° C. for 1 hour. The catalyst was removed by filtration through a ‘filter aid’ and the solvent removed to give 6-(2-aminoethanoyl)-3H-benzothiazol-2-one hydrochloride as a light brown solid (0.5 g, 96%).
Workup
- customThe catalyst was removed by filtration through a ‘
- filtrationfilter aid’ and the solvent
- customremoved
Sources & evidence
- ORD record
- ord-34ab6c7eec3748769e52d3860970fccd
- Source dataset
- uspto-grants-2003_11
- Patent number
- US06642256B2
Reaction notes
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