HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 22854555, compound → HCID 10022940, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 22854555 | HCID 22854555 | — |
| Solvent | Ammonia | HCID 222 | — |
| Product | HCID 10022940 | HCID 10022940 | 57% |
Reaction Steps
The above 2',3',5'-tri-O-benzoyl-2-chloro-N-(1-piperidinyl)adenosine (19.2 g, 27.5 mmol) was dissolved in methanolic ammonia (150 ml) (previously saturated at -10° C.) and stirred at room temperature for 18 hours. The precipitated benzamide was removed by filtration, and the filtrate was evaporated to a fawn oil, which was triturated with diethyl ether to provide the title compound (6.0 g, 57%) as a white foam, 1H NMR (400 MHz, Me2SO-d6) δ 3.55 (1H, m, H-5'a), 3.66 (1H, m, H-5'b), 3.94 (1H, q, H-4'), 4.12 (1H, m, H-3'), 4.50 (1H, q, H-2'), 5.82 (1H, d, H-1'), 8.40 (1H, s, H-8); HPLC retention time 26.57 (gradient elution, 5-25% acetonitrile/0.1M pH 3.3 ammonium sulphate buffer: 214 nm detector); purity 99%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05578582 |
| Source dataset | uspto-grants-1996_11 |
| ORD ID | ord-1326650c45cc4db581cc1b52335b7791 |
| Source note | uspto-grants-1996_11 |