HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Indanone → 4-methyl-9H-indeno[2,1-b]pyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Indanone | HCID 11983 | — |
| Reactant | But-2-yn-1-amine | HCID 12599998 | — |
| Product | 4-methyl-9H-indeno[2,1-b]pyridine | HCID 12506278 | 22% |
Reaction Steps
The title compound is prepared from indan-2-one and but-2-ynylamine following a procedure analogous to that described in Step 1 of Intermediates 1 and 2; the reaction is carried out in a microwave oven at 100° C. for 12 min. Yield: 22% of theory; LC (method 1): tR=1.98 min; Mass spectrum (ESI+): m/z=182 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08497281B2 |
| Source dataset | uspto-grants-2013_07 |
| ORD ID | ord-8ab37861528c406799e28e22ab169051 |
| Source note | uspto-grants-2013_07 |