化工社化工社 化学情報印刷レポート · 研究参考用
Ammonia → 2-Aminoadenosine
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|---|---|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Chlorotrimethylsilane | HCID 6397 | — |
| 反応物 | Guanosine Hydrate | HCID 135705230 | — |
| 溶媒 | Water | HCID 962 | — |
| 生成物 | 2-Aminoadenosine | HCID 72200 | — |
反応手順
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.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05856466 |
| 出典データセット | uspto-grants-1999_01 |
| ORD ID | ord-1cfcf0f15bc14dd4893523458c58b8b5 |
| 出典メモ | uspto-grants-1999_01 |