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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 741563Generated: October 30, 2026

Allyl iodide → Quinolizidin-2-ylmethyl-1-allylindole-3-carboxylate

https://huagongshe.com/reaction/741563

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl iodideHCID 11166—
ReactantQuinolizidin-2-ylmethylindole-3-carboxylateHCID 131719520—
ProductQuinolizidin-2-ylmethyl-1-allylindole-3-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05552398
Source datasetuspto-grants-1996_09
ORD IDord-578c3311a7584e42b37f73ef5aea75c4
Source noteuspto-grants-1996_09