Bromine → HCID 66898934, compound

HRID 19098Notes

Reaction equation

HRID 19098 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]=1

Participants

6

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

  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 (150 g silica gel 60 5% methanol/diethyl ether)
  6. 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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