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Uridine → 5'-O-(4-Methylbenzoyl)uridine

HRID 48089
Notes
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Reaction equation

HRID 48089 reaction equation
[CH3:1][C:2]1[CH:10]=[CH:9][C:5]([C:6](Cl)=[O:7])=[CH:4][CH:3]=1.[C@@H:11]1([N:20]2[CH:27]=[CH:26][C:24](=[O:25])[NH:23][C:21]2=[O:22])[O:19][C@H:16]([CH2:17][OH:18])[C@@H:14]([OH:15])[C@H:12]1[OH:13]>N1C=CC=CC=1>[CH3:1][C:2]1[CH:10]=[CH:9][C:5]([C:6]([O:18][CH2:17][C@H:16]2[O:19][C@@H:11]([N:20]3[CH:27]=[CH:26][C:24](=[O:25])[NH:23][C:21]3=[O:22])[C@H:12]([OH:13])[C@@H:14]2[OH:15])=[O:7])=[CH:4][CH:3]=1
ParticipantsProcedureWorkupSources & evidenceReaction notes

Participants

4

Reactant 2

HCID 6029UridineHCID 134054-Methylbenzoyl Chloride

Product 1

HCID 115885775'-O-(4-Methylbenzoyl)uridine

Reagents, catalysts & solvents 1

HCID 1049PyridineSolvent

Procedure

4-Methylbenzoyl chloride (10 mmol) is added to a solution of uridine (10 mmol) in 20 mL of pyridine. After no further progress occurs as observed by TLC, the volatile components are evaporated in vacuo. The residue is purified using flash chromatography to give the product as a colorless oil.

Workup

  • customthe volatile components are evaporated in vacuo
  • customThe residue is purified
  • Sources & evidence

    ORD record
    ord-5fea9a53770246ee989f9ac9adc592d9
    Source dataset
    uspto-grants-2004_03
    DOI
    10.6084/m9.figshare.5104873.v1
    Patent number
    US06702705B1

    Reaction notes

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    On this pageParticipantsProcedureWorkupSources & evidenceReaction notes