HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 53971714, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-[1-(Thiophen-2-yl)cyclopropyl]methanamine | HCID 15611175 | — |
| Reactant | HCID 53967354 | HCID 53967354 | — |
| Solvent | Formic Acid | HCID 284 | — |
| Product | HCID 53971714 | HCID 53971714 | 29% |
Reaction Steps
(1-Thien-2-ylcyclopropyl)methylamine (0.55 g, 3.6 mmol), see Example 3, 6-chloropurine-5'-deoxy-5'-chlororiboside-2',3'-isopropylidene (1.25 g, 3.6 mmol, as prepared in Example 5) and triethylamine (0.75 g, 7.5 mmol) are reacted together as described in Example 5. Aqueous formic acid hydrolysis gives 5'-chloro-5'-deoxy-N6-((1-thien-2-ylcyclopropyl)methyl)adenosine (0.44 g, 29%) as a light khaki solid foam m.p. 69°-75° C. Found: C, 50.53; H, 4.90; N, 15.90; Cl, 9.13; S, 7.22%. C18H20ClN5O3S calculated requires: C, 51.25; H, 4.74; N, 16.61; Cl, 8.42; S, 7.59%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04755594 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-d033ab34bd4a4e5ebb1938b46eb2c994 |
| Source note | uspto-grants-1988_07 |