Potassium Hydroxide → HCID 178422989, compound
Reaction equation
Br.[CH3:2][C:3]1[N:4](S(C2C=CC=CC=2)(=O)=O)[CH:5]=[C:6]([C:8]2[N:9]=[C:10]([NH:13][C:14]([NH2:16])=[NH:15])[S:11][CH:12]=2)[CH:7]=1.[OH-].[K+]>CO>[CH3:2][C:3]1[NH:4][CH:5]=[C:6]([C:8]2[N:9]=[C:10]([NH:13][C:14]([NH2:16])=[NH:15])[S:11][CH:12]=2)[CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A mixture of 12.1 g (25 mmole) of N-[4-(2-methyl-1-phenylsulfonylpyrrol-4-yl)thiazol-2-yl]guanidine hydrobromide, 12.1 g 85% potassium hydroxide and 400 ml methanol was heated at reflux for 18 hours. The mixture was cooled, evaporated to dryness, and the residue triturated with water. The resulting precipitate was collected, washed with water, and dried in vacuo to give 5.3 g (96%) of the product as its free base; m.p. 235°-237° C.
Workup
- temperaturewas heated
- temperatureat reflux for 18 hours
- temperatureThe mixture was cooled
- customevaporated to dryness
- customthe residue triturated with water
- customThe resulting precipitate was collected
- washwashed with water
- customdried in vacuo
Sources & evidence
- ORD record
- ord-7a932002ab664697a48b0870506298ef
- Source dataset
- uspto-grants-1991_06
- Patent number
- US05026715
Reaction notes
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