N-((3R,4R)-1-benzyl-4-methylpiperidin-3-yl)-2-chloro-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine → N-Methyl-N-[(3R,4R)-4-methyl-3-piperidinyl]-7H-pyrrolo[2,3-d]pyrimidin-4-amine

Temperatur

72.5 °C

To a clean, dry, nitrogen-purged 500 ml hydrogenation reactor were charged 20 wt % Pd(OH)2/C (palladium hydroxide on carbon) (5.0 g, 50% water wet), water (200 ml), and N-((3R,4R)-1-benzyl-4-methylpiperidin-3-yl)-2-chloro-N-methyl-7H-pyrrolo[2,3-d]pyrimidin-4-amine (50.0 g, 0.135 mol). The reactor was purged three times at 50 psi with nitrogen and three times at 50 psi with hydrogen. Once purging was complete, the reactor was heated to 70-75° C. and pressurized to 50 psi with hydrogen through a continuous feed. The hydrogen uptake was monitored until no hydrogen was consumed for a minimum of 1 hour. The reactor was cooled to 20-30° C. and purged three times at 50 psi with nitrogen. The reaction mixture was filtered through water-wet Celite and transferred to a clean, dry, nitrogen-purged 500 ml reactor for subsequent processing.

1. customTo a clean, dry
2. customnitrogen-purged 500 ml hydrogenation reactor
3. customThe reactor was purged three times at 50 psi with nitrogen and three times at 50 psi with hydrogen
4. customOnce purging
5. customwas consumed for a minimum of 1 hour
6. temperatureThe reactor was cooled to 20-30° C.
7. custompurged three times at 50 psi with nitrogen
8. filtrationThe reaction mixture was filtered through water-wet Celite
9. customdry
10. customnitrogen-purged 500 ml reactor for subsequent processing

ORD-Eintrag

ord-b53ac3dcf532410b9c7875238d3e143a

Quelldatensatz

uspto-grants-2012_11

DOI

10.6084/m9.figshare.5104873.v1

Patentnummer

US08309716B2