HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → HCID 22871221, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Cyclobutanone | HCID 14496 | — |
| Reactant | Sodium cyanoborohydride | HCID 5003444 | — |
| Reactant | (R)-3-(N-cyclopentylamino)-8-fluoro-5-methoxy-3,4-dihydro-2H-1-benzopyran | HCID 22871220 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | HCID 22871221 | HCID 22871221 | 53% |
Reaction Steps
To a solution of (R)-3-(N-cyclopentylamino)-8-fluoro-5- methoxy-3,4-dihydro-2H-1-benzopyran (0.9 g, 3.4 mmol), HOAc (0.22 g, 3.6 mmol) and cyclobutanone (2g, 30 mmol) in methanol (25 mL), were NaCNBH3 (1 g, 16 mmol) added in portions at room temperature. After stirring for four days GC indicated 37% product. pH was adjusted to 5 (HOAc)and additional (1 g, 15 mmol) cyclobutanone was added. After stirring for further 6 days, GC indicated 64% conversion. The solvent was evaporated and the residue worked up by extraction. Flash chromatography (EtOAc/P-ether, 1+1), gave 0.53 g (53% yield) of the title compound as a colourless oil. GC/MS (70 eV) M=319 (3%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05616610 |
| Source dataset | uspto-grants-1997_04 |
| ORD ID | ord-da13a31426dc4cfcb1856c485413f595 |
| Source note | uspto-grants-1997_04 |