Hydrochloric Acid → 2-Aminobenzothiazole-6-carboxylic acid hydrochloride
Reaction equation
[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([C:11]([O:13]CC)=[O:12])[CH:8]=[CH:7][C:5]=2[N:6]=1.[ClH:16]>>[ClH:16].[NH2:1][C:2]1[S:3][C:4]2[CH:10]=[C:9]([C:11]([OH:13])=[O:12])[CH:8]=[CH:7][C:5]=2[N:6]=1Participants
3
Procedure
500 mg of ethyl 2-aminobenzothiazole-6-carboxylate (Maybridge Co., UK) was stirred in 20 ml of 4 M hydrochloric acid at 80° C. for 5 hours. The solvent was evaporated, and the residue was washed with a solvent mixture of ethyl acetate/hexane to obtain the title compound.
Workup
- customThe solvent was evaporated
- washthe residue was washed with a solvent mixture of ethyl acetate/hexane
Sources & evidence
- ORD record
- ord-dcb7343d5ea141779291e36914b13022
- Source dataset
- uspto-grants-2004_03
- Patent number
- US06710056B2
Reaction notes
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