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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 569038Generated: October 30, 2026

Allyl bromide → HCID 13315134, compound

https://huagongshe.com/reaction/569038

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantHCID 13315133HCID 13315133—
Reactant3-(Cycloundecen-1-yl)-1,2-diazacycloundec-2-eneHCID 53630274—
SolventEthanolHCID 702—
ProductHCID 13315134HCID 13315134—

Reaction Steps

229 mg of 6-amino-3-methylthio-β-carboline are heated in 15 ml of ethanol (absolute) with 0.27 ml of allylbromide and 0.37 ml of diazabicycloundecene for 3 hours to 70° C. After concentration to dryness, it is dispersed in ethyl acetate/saturated sodium chloride solution. The organic phase is dried, filtered and concentrated. After trituration of the residue with diispropyl ether, 70 mg of 6-diallylamino-3-methylthio-β-carboline with a 110° C. melting point are obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04731358
Source datasetuspto-grants-1988_03
ORD IDord-de3ca311e09a46ca9e1c50a0389a7069
Source noteuspto-grants-1988_03