HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N6-((1-(4-chlorophenyl)cyclopropyl)methyl)adenosine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 6-Chloropurine riboside | HCID 93003 | — |
| Reactant | [1-(4-Chlorophenyl)cyclopropyl]methanamine | HCID 4120166 | — |
| Product | N6-((1-(4-chlorophenyl)cyclopropyl)methyl)adenosine | HCID 15611207 | 47% |
Reaction Steps
Reaction of the above amine (1.48 g, 8 mmol) with 6-chloropurine riboside (2.09 g, 7.3 mmol) and triethylamine (1.1 mL, 8 mmol) as prepared in Example 1 and 7 gives N6-((1-(4-chlorophenyl)cyclopropyl)methyl)adenosine (1.47 g, 47%) as a cream colored solid m.p. 132°-8° C. Found: C, 56.16; H, 5.22; N, 15.54; Cl, 9.12%. C20H22N5O4Cl calculated requires: C, 55.62; H, 5.10; N, 16.22; Cl, 8.23%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04755594 |
| Source dataset | uspto-grants-1988_07 |
| ORD ID | ord-7d0f2a7c4a6d4e8d8d3b706975eaad3f |
| Source note | uspto-grants-1988_07 |