Reaktion #715591

Reaktionsgleichung

1-methylpiperidin-3-amine

sodium tert-butoxide

(9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine)

6-benzyl-4-chloro-1,7-dimethyl-6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyridine

1-methylpiperidin-3-amine

Sodium tert-butoxide

(9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine)

→

6-benzyl-1,7-dimethyl-N-(1-methylpiperidin-3-yl)-6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyridin-4-amine

Lösungsmittel

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   Sonstigethe mixture was again degassed
2. 2
   Temperaturheating at 100° C.
3. 3
   SonstigeThe reaction mixture was partitioned between water and EtOAc
4. 4
   ExtraktionThe aqueous layer was extracted with two further portions of EtOAc
5. 5
   TrocknenThe combined organic extracts were dried over sodium sulfate
6. 6
   Filtrationfiltered
7. 7
   Einengenconcentrated
8. 8
   SonstigeThe product was purified via preparative HPLC-MS (Waters SunFire C18
9. 9
   Wascheneluting with a gradient of MeOH/H2O containing 0.1% TFA),
10. 10
    Sonstigefollowed by repurification
11. 11
    Wascheneluting with a gradient of MeCN/H2O containing 0.1% TFA),
12. 12
    Sonstigepurification
13. 13
    Wascheneluting with a gradient of MeCN/H2O containing 0.15% NH4OH)
14. 14
    Sonstigeto afford product as the free base

Vorschrift

A degassed mixture of 6-benzyl-4-chloro-1,7-dimethyl-6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyridine (25.0 mg, 0.0804 mmol, Example 228, Step 7), 1-methylpiperidin-3-amine (37 mg, 0.32 mmol, racemic, ChemBridge), Sodium tert-butoxide (15 mg, 0.16 mmol, Aldrich), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (9.3 mg, 0.016 mmol, Aldrich) and tris(dibenzylideneacetone)dipalladium(0) (7.4 mg, 0.0080 mmol, Aldrich) in toluene (1.2 mL) was heated at 100° C. overnight. Additional 1-methylpiperidin-3-amine (37 mg, 0.32 mmol), sodium tert-butoxide (15 mg, 0.16 mmol), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (46 mg, 0.080 mmol) and tris(dibenzylideneacetone)dipalladium(0) (44 mg, 0.040 mmol), were added, the mixture was again degassed and heating at 100° C. was continued for 3 hours. The reaction mixture was partitioned between water and EtOAc. The aqueous layer was extracted with two further portions of EtOAc. The combined organic extracts were dried over sodium sulfate, filtered and concentrated. The product was purified via preparative HPLC-MS (Waters SunFire C18, eluting with a gradient of MeOH/H2O containing 0.1% TFA), followed by repurification using HPLC-MS (Waters SunFire C18, eluting with a gradient of MeCN/H2O containing 0.1% TFA), again followed by a final purification using HPLC-MS (Waters XBridge C18, eluting with a gradient of MeCN/H2O containing 0.15% NH4OH) to afford product as the free base. Yield: (3 mg, 10%).

Quelle