HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 552719Generated: November 1, 2026
2,2-Dimethoxypropane → HCID 10001645, compound
https://huagongshe.com/reaction/552719
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,2-Dimethoxypropane | HCID 6495 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | p-Toluenesulfonic acid monohydrate | HCID 521998 | — |
| Reactant | N6-Benzoyladenosine | HCID 11728391 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 10001645 | HCID 10001645 | 59% |
Reaction Steps
N-{9-[(2R,3R,4S,5R)-3,4-Dihydroxy-5-(hydroxymethyl)tetrahydrofuran-2-yl]-9H-purin-6-yl}benzamide (0.643 g, 1.73 mmol), 2,2-dimethoxypropane (1.06 mL, 8.66 mmol), and para-toluenesulfonic acid monohydrate (0.333 g, 1.73 mmol) were dissolved in acetone (43 mL). The solution was stirred at room temperature overnight and then heated to 40° C. for 3 hours. Once cooled to room temperature, saturated sodium bicarbonate solution was added to the reaction mixture and then approximately half the solvent was removed in vacuo. The resulting solution was diluted with water and extracted four times with CH2Cl2. Combined organics were washed with brine and dried over Na2SO4. The crude material was purified by silica gel chromatography (0 to 5% MeOH/CH2Cl2) to isolate the title compound (0.419 g, 59%)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07951810B2 |
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| Source dataset | uspto-grants-2011_05 |
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| ORD ID | ord-fb48fd8290eb48d1bdd1f3c77947b513 |
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| Source note | uspto-grants-2011_05 |
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