HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetonitrile → HCID 131731289, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetonitrile | HCID 6342 | — |
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | HCID 131731291 | HCID 131731291 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 131731289 | HCID 131731289 | 90% |
Reaction Steps
To the thus-obtained Fmoc-t-butyl-dimethyl siloxy amide-L-proline (Compound 18) (1.18 g, 2.5 mmol), anhydrous acetonitrile (5 ml) and piperidine (2.4 ml) were added, and this was stirred for 1 hour at room temperature. After the completion of the reaction, acetonitrile (50 ml) was added to the mixture, and insoluble matters were removed by filtration. The solvent in the filtrate obtained was removed by evaporation under reduced pressure. The residual substance obtained was applied to silica gel column chromatography (the eluent: CH2Cl2: CH3OH=9:1). Thus, Compound 19 in the form of colorless syrup was obtained (0.61 g, yield: 90%). The result of NMR analysis with respect to this compound is shown below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08691782B2 |
| Source dataset | uspto-grants-2014_04 |
| ORD ID | ord-4117abc2b2b44915a1ecae8a20cf9ebc |
| Source note | uspto-grants-2014_04 |