HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → HCID 87568165, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Bromo-1-cyclopropyl-2-(2-fluorophenyl)ethan-1-one | HCID 23435871 | — |
| Reactant | HCID 87565600 | HCID 87565600 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 87568165 | HCID 87568165 | 48.5% |
Reaction Steps
Following a procedure similar to that described in Example 132-(g), (E)-4-(acetylsulfanyl)-3-{[2-(t-butoxycarbonylamino)-1,3-thiazol-4-yl]methylidene}piperidine hydrogen trifluoroacetate (420 mg) was subjected to the reaction with 2-bromo-2-(2-fluorophenyl)-1-cyclopropylethanone (340 mg) and triethylamine (310 μl) in acetonitrile (5 ml). The product obtained by usual extraction was purified by silica gel chromatography (eluent: hexane/ethylacetate=2/1˜2/3) to afford (E)-4-(acetylsulfanyl)-3-{[2-(t-butoxycarbonylamino)-1,3-thiazol-4-yl]methylidene}-1-[2-cyclopropyl-1-(2-fluorophenyl)-2-oxoethyl]piperidine (230 mg) as a pale yellow amorphous solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07829580B2 |
| Source dataset | uspto-grants-2010_11 |
| ORD ID | ord-4d62e791621f406cabc751544f4d552f |
| Source note | uspto-grants-2010_11 |