Hydrochloric Acid → HCID 178512600, compound
Reaction equation
C([O:3][C:4]([CH:6]1[C:11]2[N:12]=[C:13]([NH:15][C:16]([NH2:18])=[NH:17])[S:14][C:10]=2[CH2:9][CH2:8][CH2:7]1)=[O:5])C.[OH-].[Na+].Cl>CO.O>[NH:15]([C:13]1[S:14][C:10]2[CH2:9][CH2:8][CH2:7][CH:6]([C:4]([OH:5])=[O:3])[C:11]=2[N:12]=1)[C:16]([NH2:18])=[NH:17]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
A suspension of 2-guanidino-4,5,6,7-tetrahydro-benzothiazole-4-carboxylic acid ethyl ester (5 mmol) and sodium hydroxide (20 mmol) in methanol/water (4:1, 10 ml) is stirred overnight at room temperature. The pH is set at 5 by adding 25% hydrochloric acid and the precipitated product is filtered off. In this way the title compound is obtained (671 mg) in a yield of 56%: tR 0.64 min (LC-1); ESI-MS (+/−): m/z 241.49 [M+H]+/239.37 [M−H]−.
Workup
- filtrationthe precipitated product is filtered off
Sources & evidence
- ORD record
- ord-33413e6dcbc0448487ecea1669d7ccf7
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07727979B2
Reaction notes
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