Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2120059Generated: November 1, 2026

Pyridine → HCID 86594936, compound

https://huagongshe.com/reaction/2120059

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantAdenosine 5′-(trihydrogen diphosphate), trisodium saltHCID 12797869—
SolventDichloromethaneHCID 6344—
ProductHCID 86594936HCID 8659493698.2%

Reaction Conditions

Temperature0 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06689760B1
Source datasetuspto-grants-2004_02
ORD IDord-732c1ec22efa4d498053b3d49f60d810
Source noteuspto-grants-2004_02