Bromine → 3-(2-Methoxyethyl)-1,2,4-thiadiazol-5-amine
Reaction equation
Cl.[CH3:2][O:3][CH2:4][CH2:5][C:6]([NH2:8])=[NH:7].BrBr.C[O-].[Na+].[S-:14][C:15]#[N:16].[K+]>CO>[CH3:2][O:3][CH2:4][CH2:5][C:6]1[N:8]=[C:15]([NH2:16])[S:14][N:7]=1Participants
Conditions
- Temperature
- 5 °C
Procedure
To a solution of 3-methoxy-propionamidine hydrochloride (4.8 g, 0.035 mol) in methanol (20 mL) at 0° C. under vigorous stirring was added dropwise bromine (1.78 mL, 0.035 mol) and a 5.4M sodium methylate solution in methanol (13 mL, 0.035 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 (3.37 g, 0.035 mol) in methanol (20 mL) over 10 min at 0-10° C. The resulting mixture was stirred for 2 h at 0-10° C. and then filtered. The isolated material was washed with methanol and dried which afforded a brown solid which was purified by flash chromatography (300 g silica gel 60, 5% methanol/diethyl ether) and crystallized from diethyl ether/hexanes which afforded 3-(2-methoxy-ethyl)-[1,2,4]thiadiazol-5-ylamine (4.08 g, 74%) as a light yellow solid.
Workup
- filtrationfiltered
- washThe isolated material was washed with methanol
- customdried which
- customafforded a brown solid which
- customwas purified by flash chromatography (300 g silica gel 60, 5% methanol/diethyl ether)
- customcrystallized from diethyl ether/hexanes which
Sources & evidence
- ORD record
- ord-1afbeec922e04669a0e78cb6788857f5
- Source dataset
- uspto-grants-2010_06
- Patent number
- US07741327B2
Reaction notes
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