Toluene → Uridine pyruvate

HRID 605483

反応式

HRID 605483 の反応式
[C@@H:1]1([N:10]2[CH:17]=[CH:16][C:14](=[O:15])[NH:13][C:11]2=[O:12])[O:9][C@H:6]([CH2:7][OH:8])[C@@H:4]([OH:5])[C@H:2]1[OH:3].C1(C)C=CC=CC=1.[C:25](Cl)(=[O:29])[C:26]([CH3:28])=[O:27].CO.C(Cl)Cl>CN(C=O)C.N1C=CC=CC=1>[C:25]([O:8][CH2:7][C@H:6]1[O:9][C@@H:1]([N:10]2[CH:17]=[CH:16][C:14](=[O:15])[NH:13][C:11]2=[O:12])[C@H:2]([OH:3])[C@@H:4]1[OH:5])(=[O:29])[C:26]([CH3:28])=[O:27]

参加物

7

反応物 4

HCID 1140TolueneHCID 6029UridineHCID 5217912-Oxopropanoyl chlorideHCID 21226129Dichloromethane methanol

生成物 1

HCID 9879851Uridine pyruvate

試薬・触媒・溶媒 2

HCID 1049Pyridine溶媒HCID 6228Dimethylformamide溶媒

実験手順

Uridine (3.0 g, 12 mmol) was dried by toluene azeotrope under vacuum (3×), and then dissolved in DMF (20 mL) and pyridine (20 mL). The resultant solution was cooled to −10 degrees C. and 6.0 mL of pyruvyl chloride (produced in step A above) was added dropwise. The reaction mixture was stirred at room temperature under argon for 24 hours. Analysis by TLC (5% MeOH/CH2Cl2) showed the consumption of uridine. The reaction mixture was evaporated to dryness and partitioned between CH2Cl2 and aqueous sodium bicarbonate. The organic layer was washed with water, aqueous HCl (pH 3.0), and water; dried over sodium sulfate; —concentrated; and purified using flash chromatography (silicagel, 5% MeOH/CH2Cl2) to yield 1.4 g of uridine pyruvate, or 2′,3′,5′-tri-O-pyruvyluridine.

後処理

  1. customthe consumption of uridine
  2. customThe reaction mixture was evaporated to dryness
  3. custompartitioned between CH2Cl2 and aqueous sodium bicarbonate
  4. washThe organic layer was washed with water, aqueous HCl (pH 3.0), and water
  5. dry with materialdried over sodium sulfate
  6. customand purified

出典と根拠

ORDレコード
ord-f831d9fb4fcd4a22bd5286a182b21a57
出典データセット
uspto-grants-2011_03
特許番号
US07915233B1

関連ノート

読み込み中…