反応 #1583896

ord-bd5d8cbfa9da45b1a5a0fc33e8f424bb

溶媒

反応条件

詳細条件
See reaction.notes.procedure_details.

後処理

  1. 1
    濃縮the mixture was concentrated
  2. 2
    workup.DISSOLUTIONthe material redissolved in 40 mL DMF
  3. 3
    温度the mixture was heated at 80° C. for 1 hour
  4. 4
    温度The mixture was then cooled to room temperature
  5. 5
    その他The solution was partitioned between EtOAc (100 mL) and 50 mL 10% LiCl (aqueous)
  6. 6
    濃縮The organic layer was concentrated
  7. 7
    その他flash chromatographed 20-70% EtOAc

実験手順

Intermediate (8a) (2.4 g, 6.5 mmol) was added to 125 mL of DCM followed by DIPEA (4.6 mL, 26.1 mmol) and 4-dimethylaminopyridine (80 mg, 653 μmol). Methanesulfonyl chloride (1.0 mL, 13.1 mmol) was then added at 0° C. and the mixture was warmed to room temperature. After 3 hours, the mixture was concentrated and the material redissolved in 40 mL DMF. Sodium azide (467 mg, 7.2 mmol) was added and the mixture was heated at 80° C. for 1 hour. The mixture was then cooled to room temperature. The solution was partitioned between EtOAc (100 mL) and 50 mL 10% LiCl (aqueous). The organic layer was concentrated and flash chromatographed 20-70% EtOAc:hexanes to yield Intermediate (8b) as a yellow oil (2.1 g). MS m/z: [M+H+] calcd for C21H22FN5O2, 396.2. found 396.0.

出典

DOI: 10.6084/m9.figshare.5104873.v1特許: US09198899B2uspto-grants-2015_12