Welcome to chemicalbook!
Chinese English Japanese Germany Korea
400-158-6606
Try our best to find the right business for you.
Do not miss inquiry messages Please log in to view all inquiry messages.

Welcome back!

Benzenamine, 3-[(1-methyl-4-piperidinyl)oxy]- (9CI) synthesis

8synthesis methods
Piperidine, 1-methyl-4-(3-nitrophenoxy)-

872512-95-3
0 suppliers
inquiry

Benzenamine, 3-[(1-methyl-4-piperidinyl)oxy]- (9CI)

790667-66-2
10 suppliers
inquiry

-

Yield:790667-66-2 97%

Reaction Conditions:

with Pd/C;hydrogen in tetrahydrofuran at 20; under 775.743 Torr; for 4 h;

Steps:

3 Step 3

To a solution of 1 -methyl-4-(3-nitrophenoxy)piperidine (320 mg, 1 .35 mmol, 1 .00 eq) in tetrahydrofuran (5.00 mL) was added Pd/C 10% weight on C ( 100 mg, 1 .00 eq). The reaction was stirred under hydrogen atmosphere ( 1 5 psi) at 20°C for 4 h. The mixture was filtered, and the filtrate was concentrated under reduced pressure to afford 3-[(1 -methyl-4- piperidyl)oxy]aniline (270 mg, 1 .31 mmol, 97% yield) as a yellow solid.

References:

WO2021/69705,2021,A1 Location in patent:Page/Page column 228-229

141699-59-4 Synthesis
1-Boc-4-methanesulfonyloxypiperidine

141699-59-4
233 suppliers
$6.00/1g

Benzenamine, 3-[(1-methyl-4-piperidinyl)oxy]- (9CI)

790667-66-2
10 suppliers
inquiry

586412-88-6 Synthesis
tert-butyl 4-(3-nitrophenoxy)piperidine-1-carboxylate

586412-88-6
12 suppliers
inquiry

Benzenamine, 3-[(1-methyl-4-piperidinyl)oxy]- (9CI)

790667-66-2
10 suppliers
inquiry