Toluene → Uridine pyruvate

HRID 605483노트

반응식

HRID 605483 반응식
[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]

참가 물질

7

반응물 4

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

생성물 1

HCID 9879851Uridine pyruvate

시약·촉매·용매 2

HCID 1049Pyridine용매HCID 6228Dimethylformamide용매

실험 절차

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.

후처리

  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

출처 및 근거

ORD 기록
ord-f831d9fb4fcd4a22bd5286a182b21a57
출처 데이터셋
uspto-grants-2011_03
특허 번호
US07915233B1

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