HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Butanaminium, N,N,N-tributyl-, fluoride, hydrate → 6-Methyl-[4-{3-[3-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]prop-2-ynylidene}piperidin-1-yl]-3-nitropyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Butanaminium, N,N,N-tributyl-, fluoride, hydrate | HCID 16211673 | — |
| Reactant | 5-(3-Bromophenyl)-3-methyl-1,2,4-oxadiazole | HCID 19703124 | — |
| Reactant | 4-(3-Trimethylsilylprop-2-ynylidene)piperidine | HCID 57574982 | — |
| Reactant | 6-Methyl-3-Nitro-2-(4-prop-2-ynylidenepiperidin-1-yl)pyridine | HCID 86627349 | — |
| Product | 6-Methyl-[4-{3-[3-(3-methyl-1,2,4-oxadiazol-5-yl)phenyl]prop-2-ynylidene}piperidin-1-yl]-3-nitropyridine | HCID 86627359 | 61% |
Reaction Steps
The title Compound was prepared from Compound 274c following the procedure described for the compound of Example 274 using 5-(3-bromophenyl)-3-methyl-1,2,4-oxadiazole instead of 1-bromo-3,5-difluorobenzene and adding 1 molar equivalent of tetrabutylammonium fluoride monohydrate to the starting reaction mixture. After the work-up, the residue was purified by automated flash liquid chromatography (SP1™-Biotage) eluting with PE-EtOAc gradient from 9:1 to 7:3 affording the title product. Yellow oil. Yield: 61%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08518916B2 |
| Source dataset | uspto-grants-2013_08 |
| ORD ID | ord-4f982640478e477c946b488c7fdcb6a7 |
| Source note | uspto-grants-2013_08 |