Reaktion #715593

Reaktionsgleichung

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

tert-butyl (3R)-3-aminopyrrolidine-1-carboxylate

sodium tert-butoxide

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

→

title compound

tert-butyl (3R)-3-[(6-benzyl-1,7-dimethyl-6H-pyrrolo[2,3-e][1,2,4]triazolo[4,3-a]pyridin-4-yl)amino]pyrrolidine-1-carboxylate

Lösungsmittel

toluene

Reaktionsbedingungen

Aufarbeitung

1. 1
   SonstigeThe reaction mixture was partitioned between water and ethyl acetate
2. 2
   Extraktionthe aqueous layer was extracted further with two portions of EtOAc
3. 3
   WaschenThe combined organic extracts were washed with brine
4. 4
   Trocknendried over sodium sulfate
5. 5
   Sonstigedecanted
6. 6
   Einengenconcentrated
7. 7
   SonstigeThe product was purified by flash chromatography
8. 8
   Wascheneluting first with a gradient from 0-100% EtOAc in hexanes
9. 9
   Wascheneluting with 5% MeOH in DCM
10. 10
    SonstigeA portion of this material was then purified by preparative HPLC-MS (Waters XBridge C18
11. 11
    Wascheneluting with a gradient of MeCN/H2O containing 0.15% NH4OH)

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 (200.0 mg, 0.6435 mmol, Example 228, Step 7), tert-butyl (3R)-3-aminopyrrolidine-1-carboxylate (0.40 mL, 2.3 mmol, Aldrich), sodium tert-butoxide (190 mg, 1.98 mmol, Aldrich), (9,9-dimethyl-9H-xanthene-4,5-diyl)bis(diphenylphosphine) (93 mg, 0.16 mmol, Aldrich) and tris(dibenzylideneacetone)dipalladium(0) (74 mg, 0.080 mmol, Aldrich) in toluene (12 mL) was heated at 100° C. for 3.5 hours, then at 125° C. for 2 hours. The reaction mixture was partitioned between water and ethyl acetate, and the aqueous layer was extracted further with two portions of EtOAc. The combined organic extracts were washed with brine, dried over sodium sulfate, decanted and concentrated. The product was purified by flash chromatography, eluting first with a gradient from 0-100% EtOAc in hexanes, then eluting with 5% MeOH in DCM. Yield: (190 mg, 64%). A portion of this material was then purified by preparative HPLC-MS (Waters XBridge C18, eluting with a gradient of MeCN/H2O containing 0.15% NH4OH) to provide a pure title compound.

Quelle