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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569040Generated: October 30, 2026

Allyl bromide → HCID 20148438, compound

https://huagongshe.com/reaction/569040

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
Reactant6453-27-6HCID 317218—
Reactant3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
SolventEthanolHCID 702—
ProductHCID 20148438HCID 20148438—

Reaction Steps

360 mg of 6-amino-β-carboline are heated in 20 ml of ethanol with 0.54 ml of allylbromide and 0.74 ml diazabicycloundecene for 3 hours at 70° C. After concentration to dryness and dispersing in ethyl acetate/saturated sodium chloride solution, the organic phase is separated, dried, filtered and concentrated. The residue is chromatographed on silica gel with cyclohexane/ethyl acetate=1:1 as eluant and 50 mg of 6-diallylamino-β-carboline as oil are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731358
Source datasetuspto-grants-1988_03
ORD IDord-655dcb9f534a47d783a1c71e79b928d1
Source noteuspto-grants-1988_03