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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1899807Generated: October 31, 2026

2-Bromo-2'-chloroacetophenone → HCID 23371583, compound

https://huagongshe.com/reaction/1899807

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Bromo-2'-chloroacetophenoneHCID 2735785—
Reactant6-Methyl-2-(pyridin-4-yl)-4H-1,3,4-thiadiazin-5(6H)-oneHCID 23371618—
SolventEthanolHCID 702—
ProductHCID 23371583HCID 23371583—

Reaction Steps

6-Methyl-2-(4-pyridyl)-4H,6H-1,3,4-thiadiazin-5-one (415 mg, 2 mmol) and 2'-chlorophenacyl bromide (654 mg, 2.8 mmol) were dissolved in absolute ethanol (6 ml) and stirred at room temperature for one day. The solvent was removed under reduced pressure to obtain 1-[(2-chlorophenyl)carbonylmethyl]-4-(6-methyl-4H,6H-1,3,4-thiadiazin-5-one-2-yl)pyridinium bromide as yellow brown gum. The salt was dissolved in methanol (7 ml), gradually added with sodium borohydride (756 mg, 20 mmol) under ice cooling and stirred at room temperature overnight. The solvent was removed under reduced pressure. The residue obtained was separated by column chromatography (dichloromethane-methanol=40:1) and purified to obtain the titled compound (621 mg) as opaline plates.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05574033
Source datasetuspto-grants-1996_11
ORD IDord-8c934919e8a049f7937d9b3da4fa11e3
Source noteuspto-grants-1996_11