Bromine → 3-(2-Methoxyethyl)-1,2,4-thiadiazol-5-amine

HRID 19095Notes

Reaction equation

HRID 19095 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]=1

Participants

6

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

  1. filtrationfiltered
  2. washThe isolated material was washed with methanol
  3. customdried which
  4. customafforded a brown solid which
  5. customwas purified by flash chromatography (300 g silica gel 60, 5% methanol/diethyl ether)
  6. 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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