HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Chloroquinoline → 2-{4-[(4-Tert-butylphenyl)sulfonyl]piperidin-1-yl}quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Chloroquinoline | HCID 11928 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-[(4-Tert-butylphenyl)sulfonyl]piperidine | HCID 18538636 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-{4-[(4-Tert-butylphenyl)sulfonyl]piperidin-1-yl}quinoline | HCID 68548007 | 18% |
Reaction Steps
Using the procedure from Example 7A, 4-[(4-tert-butylphenyl)sulfonyl]piperidine (150 mg, 0.53 mmol) was reacted with 2-chloroquinoline (175 mg, 1.06 mmol), DIEA (0.37 ml, 2.12) and 1,4-dioxane (0.2 ml) at 185° C. to afford the title compound (39 mg), a white solid, in 18% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07632838B2 |
| Source dataset | uspto-grants-2009_12 |
| ORD ID | ord-046085e83c6841848bfcdc0f7ab1a11e |
| Source note | uspto-grants-2009_12 |