HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 69489389, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | HCID 58860668 | HCID 58860668 | — |
| Solvent | Ethanol | HCID 702 | — |
| Solvent | Acetonitrile--water (1/1) | HCID 18373917 | — |
| Product | HCID 69489389 | HCID 69489389 | 104.2% |
Reaction Steps
Add a solution of acetyl chloride (0.144 mL, 2.02 mmol) in absolute ethanol to a solution of (S)-9-fluoro-5-{3-[2-(4-methoxy-phenyl)-ethyl]-4-methyl-piperazin-1-yl}-11H-12-thia-6,11-diaza-dibenzo[a,f]azulene (0.174 g, 0.348 mmol) in absolute ethanol and stir briefly at ambient temperature. Concentrate solution under reduced pressure to give an orange solid. Reconstitute the solid in acetonitrile: water (1:1), freeze-dry the solution in a dry-ice/acetone bath, and lyophilize overnight to give the title compound (0.208 g) as a yellow solid: mass spectrum (APCI+, m/e): 501 (M+1–2HCl); exact mass spectrum (ES+, m/e, C29H29FN4OS.2HCl): calc. 501.2124 (M+1–2HCl), found 501.2130.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07214673B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-c12249f49b9f4f9589fee4048ce12638 |
| Source note | uspto-grants-2007_05 |