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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1439860Generated: November 2, 2026

Allyl bromide → HCID 18984426, compound

https://huagongshe.com/reaction/1439860

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 numberUS05496815
Source datasetuspto-grants-1996_03
ORD IDord-92ee07872ce2408383253fbcc67af996
Source noteuspto-grants-1996_03