Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Adenosine 5′-(trihydrogen diphosphate), trisodium salt | HCID 12797869 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86594936 | HCID 86594936 | 98.2% |
Reaction Steps
To a 500 mL round-bottomed flask was added 3 g (21.7 mmol) adenosine-5′-diphosphate sodium salt and 200 mL pyridine. After the salt had dissolved. the solution was cooled to 0° C. under nitrogen atmosphere. Trimethylsilyl chloride (85 g, 800 mmol) in 200 mL dichloromethane was added slowly to the solution. After this addition was complete, the reaction was stirred at 35° C. for 8 hr. The pyridine hydrochloride salt was removed by filtration and excess pyridine and dichloromethane removed under high vacuum for 24 hr to yield 19.3 g (21.3 mmol) of TMS-ADP. The product was used without further purification. This synthesis is illustrated in FIG. 4E.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06689760B1 |
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| Source dataset | uspto-grants-2004_02 |
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| ORD ID | ord-732c1ec22efa4d498053b3d49f60d810 |
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| Source note | uspto-grants-2004_02 |
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