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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Bromo-2'-chloroacetophenone | HCID 2735785 | — |
| Reactant | 6-Methyl-2-(pyridin-4-yl)-4H-1,3,4-thiadiazin-5(6H)-one | HCID 23371618 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 23371583 | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US05574033 |
|---|
| Source dataset | uspto-grants-1996_11 |
|---|
| ORD ID | ord-8c934919e8a049f7937d9b3da4fa11e3 |
|---|
| Source note | uspto-grants-1996_11 |
|---|