HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 15611191, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Phenylcyclopropanemethanamine | HCID 70287 | — |
| Reactant | 6-Chloropurine riboside | HCID 93003 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 15611191 | HCID 15611191 | 79% |
Reaction Steps
A mixture of 6-chloropurine riboside (8.61 g, 30 mmol), (1-phenylcyclopropyl)methylamine (4.41 g, 30 mmol) and triethylamine (6.06 g, 60 mmol) are refluxed in stirring ethanol (300 mL) under N2 for 20 h. On cooling to 0° the product crystallized. Vacuum filtration and drying in vacuo gives N6-((1-phenylcyclopropyl)methyl)adenosine (9.24 g, 79%) as a very pale khaki solid m.p. 118°-23° C. Found: C, 59.58; H, 5.77; N, 17.49%. C20H23N5O4 calculated requires: C, 60.45; H, 5.79; N, 17.63%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04755594 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-7a022ce9ea4e439d8f387823892afc08 |
| Source note | uspto-grants-1988_07 |