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tert-Butyl 4-((cyanoMethyl)aMino)piperidine-1-carboxylate synthesis

3synthesis methods
87120-72-7 Synthesis
4-Amino-1-Boc-piperidine

87120-72-7
28 suppliers
$6.00/1g

tert-Butyl 4-((cyanoMethyl)aMino)piperidine-1-carboxylate

1224923-48-1
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Yield:1224923-48-1 295 mg

Reaction Conditions:

with potassium carbonate in acetonitrile at 80; for 23 h;

Steps:

Intermediate 7 (INT 7)

A mixture of tert-butyl 4-aminopiperidine-1-carboxylate (303 mg, 1.51 mmol) , 2-chloroacetonitrile (121 mg, 1.60 mmol) and K 2CO 3 (420 mg, 3.04 mmol) in ACN (10 mL) was heated to 80 for 23 h. The mixture was filtered and concentrated. The residue was purified by silica gel chromatography (eluting with 0-35 %DCM /MeOH) to provide INT 7 (295 mg) . MS m/z 240 [M+H] +.

References:

WO2022/105855,2022,A1 Location in patent:Page/Page column 152

87120-72-7 Synthesis
4-Amino-1-Boc-piperidine

87120-72-7
28 suppliers
$6.00/1g

590-17-0 Synthesis
Bromoacetonitrile

590-17-0
326 suppliers
$5.00/5g

tert-Butyl 4-((cyanoMethyl)aMino)piperidine-1-carboxylate

1224923-48-1
4 suppliers
inquiry