反应详情

温度

100 °C

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.

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