HuagongsheHuagongshe Chemistry Print Report · For research reference only
Allyl iodide → Quinolizidin-2-ylmethyl-1-allylindole-3-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Allyl iodide | HCID 11166 | — |
| Reactant | Quinolizidin-2-ylmethylindole-3-carboxylate | HCID 131719520 | — |
| Product | Quinolizidin-2-ylmethyl-1-allylindole-3-carboxylate | HCID 131719527 | — |
Reaction Steps
eq-Quinolizidin-2-ylmethylindole-3-carboxylate (E9b) was alkylated with allyl iodide using the method in Example 18. The product was chromatographed on silica gel eluting initially with ether, then with ethyl acetate, to afford the title compound (E19) as a colourless oil. This was converted to its hydrochloride salt mp 190°-192° C. (acetone)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05552398 |
| Source dataset | uspto-grants-1996_09 |
| ORD ID | ord-578c3311a7584e42b37f73ef5aea75c4 |
| Source note | uspto-grants-1996_09 |