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1021018-03-0

4-(1-methyl-1H-tetrazol-5-yl)piperidine synthesis

6synthesis methods
tert-butyl 4-(1-methyl-1H-tetrazol-5-yl)piperidine-1-carboxylate

1269429-34-6
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4-(1-methyl-1H-tetrazol-5-yl)piperidine

1021018-03-0
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Yield:1021018-03-0 95%

Reaction Conditions:

with hydrogenchloride in 1,4-dioxane at 20; for 1 h;

Steps:

11.B; 12.B

Step B: 4-(l -methyl- lH-tetrazol- 5 -yl)piperidine (i-11); The isomer 1 from Step A above (45 mg, 0.16 mmol) was dissolved in 4 M HC1 in dioxane (1.0 mL) and stirred at RT for 1 h. The product was concentrated under reduced pressure and dried under high vacuum to give the title compound (i-l 1) (25 mg, 95%). ESI-MS calculated for T-I^Ns: Exact Mass: 167.13; Found 168.12.

References:

WO2012/12314,2012,A1 Location in patent:Page/Page column 55

1401728-91-3 Synthesis
1-benzyl-4-(1-methyl-1H-tetrazol-5-yl)piperidine

1401728-91-3
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4-(1-methyl-1H-tetrazol-5-yl)piperidine

1021018-03-0
4 suppliers
inquiry