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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 241486Generated: October 26, 2026

Pyridine → HCID 54357673, compound

https://huagongshe.com/reaction/241486

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantChloroacetyl chlorideHCID 6577—
ReactantLuminolHCID 10638—
SolventAcetic acid 10-acetoxymethyl-anthracen-9-ylmethyl esterHCID 613145—
ProductHCID 54357673HCID 54357673—

Reaction Steps

Luminol (1.55 g; 8.75 mmol) was reacted with 2-chloro-acetylchloride (1.24 g; 10.99 mmol), in the presence of pyridine (1.07 g, 13.6 mmol) in acetic:acid (45 ml). Contents were stirred and refluxed for 1 h, allowed to cool to RT, and transferred to a refrigerator for precipitation of the product to obtain 2-Chloro-N-(1,4-dioxo-1,2,3,4-tetrahydrophthalazine-5-yl)acetamide. Thereafter, acetic acid (20 ml) was added to the cold precipitates prior to filtration (for uniform transfer into the filtration unit). Finally, precipitates were filtered, washed with methylene chloride (three times) and dried under vacuum to yield 2-Chloro-N-(1,4-dioxo-1,2,3,4-tetrahydrophthalazine-5-yl)acetamide (1.6 g; 6324 mmol; 72.2%). 1H NMR (300 MHz, DMSO-d6) δ: 8.82-8.87 (t, 1H), 7.71-7.89 (dd, 1H), 7.61-7.69 (dd, 1H), 4.34 (s, 2H), 2.16 (s, 3H, Methyl for Acetic Acid); ESMS: Calcd for C10H8ClN3O3: 253.0, Found, 253.8.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08652442B2
Source datasetuspto-grants-2014_02
ORD IDord-1fe4a8b7ba31481dbb6c6ea70e14ba5d
Source noteuspto-grants-2014_02