Bromine → HCID 66898934, compound
Reaction equation
Cl.[F:2][C:3]([F:10])([F:9])[CH2:4][CH2:5][C:6]([NH2:8])=[NH:7].BrBr.C[O-].[Na+].[S-:16][C:17]#[N:18].[K+]>CO>[F:2][C:3]([F:10])([F:9])[CH2:4][CH2:5][C:6]1[N:8]=[C:17]([NH2:18])[S:16][N:7]=1Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 5 °C
Procedure
To a solution of 4,4,4-trifluoro-butyramidine hydrochloride (2.1 g, 0.012 mol) in methanol (10 mL) at 0° C. under vigorous stirring was added dropwise bromine (0.61 mL, 0.012 mol) and a 5.4M sodium methylate solution in methanol (4.4 mL, 0.012 mol) simultaneously over 30 min maintaining a slight bromine excess by color. To the resulting nearly colorless suspension was added dropwise a solution of potassium thiocyanate (1.16 g, 0.012 mol) in methanol (10 mL) over 10 min at 0-10° C. The resulting mixture was stirred for 2 h at 0-10° C. and filtered. The isolated material was washed with methanol and dried which afforded a brown solid which was purified by flash chromatography (150 g silica gel 60 5% methanol/diethyl ether) and crystallized from diethyl ether/hexanes which afforded 3-(3,3,3-trifluoro-propyl)-[1,2,4]thiadiazol-5-ylamine (1.43 g, 61%) as a brown oil.
Workup
- filtrationfiltered
- washThe isolated material was washed with methanol
- customdried which
- customafforded a brown solid which
- customwas purified by flash chromatography (150 g silica gel 60 5% methanol/diethyl ether)
- customcrystallized from diethyl ether/hexanes which
Sources & evidence
- ORD record
- ord-9e10b8a9f5554c7881fca353d52876dc
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07741327B2
Reaction notes
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