Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Butanethiol | HCID 8012 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | HCID 10215392 | HCID 10215392 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 67211057 | HCID 67211057 | — |
Reaction Steps
20 μl (0.115 mmol; 1.2 eq.) of diisopropylethylamine and 16 μl (0.154 mmol; 1.6 eq.) of butanethiol are added to 33 mg (96 μmol) of the compound of Example 35 in solution in 4 ml of anhydrous ethanol. The reaction mixture is maintained under stirring for 24 hours at 60° C., then after concentration under reduced pressure, the residue is purified by chromatography on a silica column (eluent: dichloromethane/methanol 95/5) and the expected product is obtained, after taking up in ethyl ether, in the form of a violet-coloured powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07495021B2 |
|---|
| Source dataset | uspto-grants-2009_02 |
|---|
| ORD ID | ord-2858fa6bc35d42c7802ac1cddba65bd1 |
|---|
| Source note | uspto-grants-2009_02 |
|---|