HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Anhydride → HCID 123182536, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 87374061 | HCID 87374061 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 123182536 | HCID 123182536 | — |
Reaction Steps
To a solution of rac-6-[(6-chloropyridin-3-yl)methyl]-3-[trans-2-hydroxycyclohexyl]benzo[h]quinazolin-4(3H)-one (0.040 g, 0.095 mmol) in 2 mL of CH2Cl2 at 0° C. was added acetic anhydride (0.011 mL, 0.11 mmol) and triethylamine (0.026 mL, 0.20 mmol). The mixture was warmed to rt and after 15 h, concentrated in vacuo. The residue was purified via preparative reverse phase HPLC to provide the title compound that gave a proton NMR spectra consistent with theory and a mass ion (ES+) of 461.9 for [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08883810B2 |
| Source dataset | uspto-grants-2014_11 |
| ORD ID | ord-6229eea7accb48819e78b58a041c1e57 |
| Source note | uspto-grants-2014_11 |