Hydrazine → HCID 18660584, compound

HRID 325068Notes

Reaction equation

HRID 325068 reaction equation
C1(=O)[N:5]([CH2:6][CH2:7][CH2:8][O:9][C@@H:10]2[C@H:14]([OH:15])[C@@H:13]([CH2:16][OH:17])[O:12][C@H:11]2[N:18]2[CH:25]=[C:24]([CH3:26])[C:22](=[O:23])[NH:21][C:19]2=[S:20])C(=O)C2=CC=CC=C12.NN>CO>[NH2:5][CH2:6][CH2:7][CH2:8][O:9][C@@H:10]1[C@H:14]([OH:15])[C@@H:13]([CH2:16][OH:17])[O:12][C@H:11]1[N:18]1[CH:25]=[C:24]([CH3:26])[C:22](=[O:23])[NH:21][C:19]1=[S:20]

Participants

4

Reactant 2

HCID 9321HydrazineHCID 18660586Uridine, 2′-O-[3-(1,3-dihydro-1,3-dioxo-2H-isoindol-2-yl)propyl]-5-methyl-2-thio-

Product 1

HCID 18660584HCID 18660584, compound

Reagents, catalysts & solvents 1

HCID 887MethanolSolvent

Conditions

Temperature
62.5 °C

Procedure

2′-O-Phthalimidopropyl-5-methyl-2-thiouridine (5.0 g, 15.8 mmol) is dissolved in 100 ml methanol in a 500 ml flask. Hydrazine (2.02 g, 63.2 mmol) is added and the mixture is heated to reflux (60-65° C.) with stirring for 14 hours. The solvent is evaporated in vacuo and the residue is dissolved in dichloromethane (150 ml) and extracted twice with an equal volume NH4OH. The organic layer is evaporated to yield the crude product. NMR is used to assay product purity. The product is used in subsequent reactions without further purification.

Workup

  1. temperaturethe mixture is heated
  2. customThe solvent is evaporated in vacuo
  3. dissolutionthe residue is dissolved in dichloromethane (150 ml)
  4. extractionextracted twice with an equal volume NH4OH
  5. customThe organic layer is evaporated

Sources & evidence

ORD record
ord-b4c3b296f8474dcaa14dc364a08ba0fb
Source dataset
uspto-grants-2001_04
Patent number
US06222025B1

Reaction notes

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