HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1270232Generated: October 30, 2026
Sodium Bicarbonate → HCID 11231258, compound
https://huagongshe.com/reaction/1270232
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 2-Acetoxyisobutyryl bromide | HCID 2724715 | — |
| Reactant | HCID 11174104 | HCID 11174104 | — |
| Reactant | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 11231258 | HCID 11231258 | 115% |
Reaction Steps
To a mixture of 2-amino-7-(β-D-ribofuranosyl)-4-chloro-7H-pyrrolo[2,3-d]pyrimidine (1.8 g, 6.0 mmol) in acetonitrile (80 mL) were added a solution of H2O/CH3CN (1:9, 1.08 mL) and then α-acetoxyisobutyryl bromide (3.5 mL, 24 mmol). After 2 h stirring at room temperature, saturated aqueous NaHCO3 (170 mL) was added and the mixture was extracted with EtOAc (300+200 mL). The combined organic phase was washed with brine (100 mL), dried (Na2SO4) and evaporated to a pale yellow foamy residue. This was suspended in anhydrous MeOH (80 mL) and stirred overnight with 25 mL of DOWEX OH− resin (previously washed with anhydrous MeOH). The resin was filtered, washed thoroughly with MeOH and the combined filtrate evaporated to give a pale yellow foam (1.92 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07202224B2 |
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| Source dataset | uspto-grants-2007_04 |
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| ORD ID | ord-a6451810bb454124a511e9ff1dab1e3b |
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| Source note | uspto-grants-2007_04 |
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