HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Aminoquinoline → Z-Val-Pro 6-aminoquinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Aminoquinoline | HCID 11373 | — |
| Reactant | Diisopropylcarbodiimide | HCID 12734 | — |
| Reactant | 1-Hydroxybenzotriazole | HCID 75771 | — |
| Reactant | Z-Val-pro-OH | HCID 10783923 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Z-Val-Pro 6-aminoquinoline | HCID 131729872 | — |
Reaction Steps
A solution of Z-Val-Pro-OH (217.4 mg, 0.62 mmol) in dichloromethane (1.5 mL), was successively treated at room temperature. with 1-hydroxibenzotriazol (84.3 mg, 0.62 mmol), N,N′-diisopropylcarbodiimide (97.2 μL, 0.62 mmol) and 6-aminoquinoline (75 mg, 0.52 mmol). The stirring was continued until the complete disappearance of the starting material (overnight). Then, the solvent was evaporated, the residue was dissolved in ethyl acetate and washed with citric acid (10%), NaHCO3 (10%) and brine. The organic layer was dried (Na2SO4) and evaporated leaving a residue that was purified by CCTLC on the chromatotron with hexane/ethyl acetate (1:4) to yield H (20 yield
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08236756B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-837f8df55324406d983aa5ce7878dffa |
| Source note | uspto-grants-2012_08 |