HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diethyl Sulfate → HCID 13137009, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diethyl Sulfate | HCID 6163 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Tetrafluoro-m-phenylenediamine dihydrochloride | HCID 149026 | — |
| Reactant | HCID 13137007 | HCID 13137007 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 13137009 | HCID 13137009 | — |
Reaction Steps
Prepared by the method described in Example 37 from 3-[2-(diethylamino)propyl]-1,2,3,4-tetrahydro-8,9-dihydroxy-5H-[1]benzopyrano[3,4-c]pyridin-5-one dihydrobromide (17.0 g, 0.034 moles), potassium carbonate (27.6 g, 0.20 moles), and diethyl sulfate (20.0 g, 0.13 moles). The crude free base product is converted to the dihydrochloride in absolute ethanol. A second recrystallization from ethanol yielded the final product (1.8 g), mp 148°-152° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04382939 |
| Source dataset | uspto-grants-1983_05 |
| ORD ID | ord-5098c1c0d8c141bd89e235addf461b08 |
| Source note | uspto-grants-1983_05 |