HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Ethynylcyclohexanol → HCID 15172931, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Ethynylcyclohexanol | HCID 6525 | — |
| Reactant | Ethynylcyclohexane | HCID 70263 | — |
| Reactant | 2-Iodoadenosine | HCID 169662 | — |
| Product | HCID 15172931 | HCID 15172931 | 79% |
Reaction Steps
The procedure of Example 1 was repeated except that 1.14 g (2.9 mmol) of 2-iodoadenosine was used as the starting compound, that the cyclohexylacetylene was replaced by 1-ethynyl-1-cyclohexanol, and that the reaction was carried out at a temperature of 100° C. for one hour, respectively, whereby 0.91 g (2.3 mmol) of crystalline 2-[(1-hydroxycyclohexane-1-yl)ethynyl]adenosine was obtained (yield: 79%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05189027 |
| Source dataset | uspto-grants-1993_02 |
| ORD ID | ord-86dce0ae6ea04b2c9a12325e501045fc |
| Source note | uspto-grants-1993_02 |