Methanol → HCID 10643625, compound

HRID 2271254Notes

Reaction equation

HRID 2271254 reaction equation
[CH2:1]([Si:3]([C:8]#[C:9][C@:10]1([CH2:32][O:33]CC2C=CC=CC=2)[O:14][C@@H:13]([N:15]2[CH:22]=[CH:21][C:19](=[O:20])[NH:18][C:16]2=[O:17])[C@H:12]([OH:23])[C@@H:11]1[O:24]CC1C=CC=CC=1)([CH2:6][CH3:7])[CH2:4][CH3:5])[CH3:2].B(Cl)(Cl)Cl.N1C=CC=CC=1.CO>ClCCl>[CH2:1]([Si:3]([C:8]#[C:9][C@:10]1([CH2:32][OH:33])[O:14][C@@H:13]([N:15]2[CH:22]=[CH:21][C:19](=[O:20])[NH:18][C:16]2=[O:17])[C@H:12]([OH:23])[C@@H:11]1[OH:24])([CH2:4][CH3:5])[CH2:6][CH3:7])[CH3:2]

Participants

6

Reactant 4

HCID 887MethanolHCID 1049PyridineHCID 25135Boron TrichlorideHCID 107455044'-C-triethylsilylethynyl-3',5'-di-O-benzyluridine

Product 1

HCID 10643625HCID 10643625, compound

Reagents, catalysts & solvents 1

HCID 6344DichloromethaneSolvent2×

Procedure

Compound 8 (1.50 g, 2.67 mmol) was dissolved in dichloromethane (75.0 ml), and a 1.0 M boron trichloride (26.7 ml, 26.7 mmol) in dichloromethane was added to the solution at −78° C. in an argon atmosphere, followed by stirring for three hours at the same temperature. A mixture of pyridine (10.0 ml) and methanol (20.0 ml) was added thereto at −78° C., followed by stirring for ten minutes. The reaction mixture was concentrated through distillation under reduced pressure, and the residue was partitioned with ethyl acetate and water. The organic layer was dried over anhydrous magnesium sulfate and concentrated through distillation under reduced pressure. The residue was purified by means of silica gel column chromatography (silica gel 200 ml, eluent; chloroform:methanol=9:1), to thereby yield a white powdery compound (Compound 9; 0.95 g, 2.48 mmol, 92.9%).

Workup

  1. additionwas added
  2. customat −78° C.
  3. stirringby stirring for ten minutes
  4. concentrationThe reaction mixture was concentrated through distillation under reduced pressure
  5. customthe residue was partitioned with ethyl acetate and water
  6. dry with materialThe organic layer was dried over anhydrous magnesium sulfate
  7. concentrationconcentrated through distillation under reduced pressure
  8. customThe residue was purified by means of silica gel column chromatography (silica gel 200 ml, eluent; chloroform:methanol=9:1)

Sources & evidence

ORD record
ord-cacddde5f77d42cdab1f46098db3e78a
Source dataset
uspto-grants-2001_12
Patent number
US06333315B1

Reaction notes

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