HuagongsheHuagongshe Chemistry Print Report · For research reference only
Ethyl Acetate → HCID 58149933, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 2-Chloroquinoline | HCID 11928 | — |
| Reactant | HCID 66877400 | HCID 66877400 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 58149933 | HCID 58149933 | 8% |
Reaction Steps
The contents of the three vials were pooled with the reaction mixture from a previous preparation of D6 (using the same method and 100 mg of chloroquinoline starting material), and the mixture diluted with ethyl acetate and washed sequentially with brine (×2) and water (×2). The organic layers were concentrated in vacuo to give a red oil that was dissolved in dichloromethane, and purified by flash chromatography on silica gel, eluting with a dichloromethane/ethyl acetate (2% to 20% EtOAc) gradient. The relevant fractions were pooled and concentrated in vacuo to give a red solid that was triturated with diethyl ether. The resulting brick coloured solid was collected by filtration and dried in vacuo to give the title compound (80 mg, 8%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08329730B2 |
| Source dataset | uspto-grants-2012_12 |
| ORD ID | ord-d707b9979b0e4a46be77afaaac5660dd |
| Source note | uspto-grants-2012_12 |