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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1066404Generated: October 27, 2026

Ammonia → 2-Aminoadenosine

https://huagongshe.com/reaction/1066404

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 generated 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 evaporation, or open and re-seal the Parr bomb under a dry nitrogen atmosphere.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06242592B1
Source datasetuspto-grants-2001_06
ORD IDord-19461fa2877d4dbe8ffdc509e3ae2b58
Source noteuspto-grants-2001_06