HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 2-Butyryl-6-methoxy-3,3,14-trimethyl-3,14-dihydro-7H-benzo[b]-chromeno[6,5-g][1,8]naphthyridin-7-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Butyryl chloride | HCID 8855 | — |
| Reactant | Aluminum(III) Chloride | HCID 6451240 | — |
| Reactant | HCID 68586536 | HCID 68586536 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 2-Butyryl-6-methoxy-3,3,14-trimethyl-3,14-dihydro-7H-benzo[b]-chromeno[6,5-g][1,8]naphthyridin-7-one | HCID 68587361 | — |
Reaction Steps
A mixture of 0.81 mmol of butyryl chloride and 0.673 mmol of AlCl3 in 2 ml of anhydrous dichloromethane is added in small portions to 0.135 mmol of the product of Example 2 in 2 ml of dichloromethane at 0° C. The reaction mixture is stirred for 4 hours at ambient temperature and then poured into a 10% solution of HCl. Following conventional treatment of the organic phases, and evaporation thereof under reduced pressure, chromatography of the residue on silica gel (dichloromethane/methanol gradient) allows the expected product to be isolated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741325B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-7f7b339957f84bd1aa5608085f6c63b5 |
| Source note | uspto-grants-2010_06 |