Trimethylsilyl triflate → 5-Aza-2'-deoxycytidine
反応式
FC(F)(F)C(=N[Si](C)(C)C)O[Si](C)(C)C.[NH:16]1[CH:23]=[N:22][C:20]([NH2:21])=[N:19][C:17]1=[O:18].C[Si](OS(C(F)(F)F)(=O)=O)(C)C.Cl[C:37]1([O:43][C@H:42]([CH:44](C(C2C=CC(C)=CC=2)=O)[OH:45])[C@@:40](C(C2C=CC(C)=CC=2)=O)([OH:41])[CH2:39]1)O.C[O-].[Na+]>C(#N)C.CO>[CH2:39]1[C@H:37]([N:16]2[C:17](=[O:18])[N:19]=[C:20]([NH2:21])[N:22]=[CH:23]2)[O:43][C@H:42]([CH2:44][OH:45])[C@H:40]1[OH:41]参加物
反応物 5
生成物 1
試薬・触媒・溶媒 2
実験手順
34 mL of BSTFA are added to a suspension of 6.4 g of azacytosine in 300 mL of acetonitrile. The mixture is brought to 50° C. and it is stirred for 90 minutes. It is cooled to ambient temperature, 6.3 mL of trimethylsilyltriflate and 11.1 g of 1-chloro-3,5-di-p-toluoyl-2-deoxy-D-ribofuranose are added to the solution, in about ten minutes. It is stirred for 140 minutes, 400 mL of methanol are added controlling the temperature in an ice bath. Concentration is carried out at low pressure until a viscous residue is obtained, 400 mL of methanol are added, it is heated to 50° C. and 36 mL of 30% solution of sodium methylate in methanol are added. It is stirred for 1 hour, it is cooled to 0° C., it is stirred to complete precipitation and the solid is filtered by washing it on the filter with methanol. 2.3 g of decitabine with HPLC purity (UV 254 nm) of 99.2% are obtained after drying at low pressure.
後処理
- customis brought to 50° C.
- stirringIt is stirred for 140 minutes
- concentrationConcentration
- customis obtained
- temperatureit is heated to 50° C.
- stirringIt is stirred for 1 hour
- temperatureit is cooled to 0° C.
- stirringit is stirred to complete precipitation
- filtrationthe solid is filtered
- washby washing it on the
- filtrationfilter with methanol
出典と根拠
- ORDレコード
- ord-208bd4b0488f4fc3b89b3c2da543ecc0
- 出典データセット
- uspto-grants-2016_02
- 特許番号
- US09266863B2
反応ノート
読み込み中…