HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ammonia → 2-Aminoadenosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Chlorotrimethylsilane | HCID 6397 | — |
| Reactant | Guanosine Hydrate | HCID 135705230 | — |
| Solvent | Water | HCID 962 | — |
| Product | 2-Aminoadenosine | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05646265 |
| Source dataset | uspto-grants-1997_07 |
| ORD ID | ord-494fc1639bc14d2596e0d0c070bd9931 |
| Source note | uspto-grants-1997_07 |