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5-(4-METHYLPIPERAZIN-1-YL)-1,3,4-THIADIAZOL-2-AMINE synthesis

1synthesis methods
109-01-3 Synthesis
1-Methylpiperazine

109-01-3
645 suppliers
$5.00/5G

37566-39-5 Synthesis
2-AMINO-5-BROMO-[1,3,4]THIADIAZOLE

37566-39-5
214 suppliers
$24.00/10g

5-(4-METHYLPIPERAZIN-1-YL)-1,3,4-THIADIAZOL-2-AMINE

71125-50-3
8 suppliers
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Yield:71125-50-3 53%

Reaction Conditions:

in propan-1-ol at 100; for 8 h;Sealed tube;

Steps:

Synthesis of 5-(4-methylpiperazin-1-yl)-1,3,4-thiadiazol-2-amine (Precursor-21)

5-Bromo-1,3,4-thiadiazol-2-amine 40 (2.20 g, 12.29 mmol) and 1- methylpiperazine (2.46 g, 24.6 mmol) were heated in n-propanol (30 mL) in a sealed tube at 100°C for 8 h. The reaction was cooled to rt, solvents evaporated under reduced pressure and the crude obtained was triturated with MeOH to obtain 5-(4- methylpiperazin-l-yl)-1,3,4-thiadiazol-2-amine precursor-21 (1.3 g, 53% yield) as an off white solid. MS: 200.16 (M+H).

References:

WO2015/25197,2015,A1 Location in patent:Paragraph 000111