Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1198448Generated: October 31, 2026

Allyl bromide → HCID 18984426, compound

https://huagongshe.com/reaction/1198448

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAllyl bromideHCID 7841—
ReactantPotassium CarbonateHCID 11430—
ReactantHCID 18984401HCID 18984401—
SolventAcetoneHCID 180—
ProductHCID 18984426HCID 18984426—

Reaction Steps

To a mixture of 3-(4-chlorophenyl)-1-[3-(methylamino)propyl]-1H-naphtho[2,1-b][1,4]thiazin-2(3H)-one (1.79 g), potassium carbonate (2.18 g) and acetone (50 ml) is added allyl bromide (0.65 g) under ice cooling, and the mixture is stirred at room temperature overnight. The insoluble materials are filtered off and acetone is distilled off, and the oily residue is purified by silica gel column chromatography (eluent, chloroform: methanol=20:1) to give 1-[3-(N-allyl-N-methylamino)propyl]-3-(4-chlorophenyl)-1H-naphtho-[2,1-b][1,4]thiazin-2(3H)-one as oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05281592
Source datasetuspto-grants-1994_01
ORD IDord-91643836807c45be8100323a4d453a4c
Source noteuspto-grants-1994_01