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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2212474Generated: October 30, 2026

Ammonia → 2-Aminoadenosine

https://huagongshe.com/reaction/2212474

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantChlorotrimethylsilaneHCID 6397—
ReactantGuanosine HydrateHCID 135705230—
SolventWaterHCID 962—
Product2-AminoadenosineHCID 72200—

Reaction Steps

This variation of the procedures of Robins, et al. supra, eliminated the need to utilize liquid ammonia in the reaction mixture since the ammonia molecule is generation in situ from the silazane reagent and the water of hydration of the guanosine hydrate starting material. Further, the use of chlorotrimethylsilane was not necessary nor was it necessary to conduct the reaction under anhydrous conditions, do a preliminary evaportaion, or open and re-seal the Parr bomb under a dry nitrogen atmosphere.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07101993B1
Source datasetuspto-grants-2006_09
ORD IDord-3ff4d942f8874591acd4a4f4ae544b4b
Source noteuspto-grants-2006_09