Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2357538Generated: November 1, 2026

Phosphorus oxychloride → 3-(1-chlorophthalazin-6-yl)-N-cyclopropyl-4-methylbenzamide

https://huagongshe.com/reaction/2357538

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPhosphorus oxychlorideHCID 24813—
ReactantCyclopropylamineHCID 69828—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 178425877HCID 178425877—
Product3-(1-chlorophthalazin-6-yl)-N-cyclopropyl-4-methylbenzamideHCID 1184831250.2%

Reaction Conditions

Temperature80 °C

Reaction Steps

A suspension of 3-(1-hydroxyphthalazin-6-yl)-4-methylbenzoic acid (1.0 g, 3.6 mmol) in phosphorous oxychloride (4.9 mL, 54 mmol) was heated at 80° C. for 1 h. The solution was cooled and concentrated. Toluene (10 mL) was added and removed in vacuo. The brown syrup was resuspended in DCM (20 mL) and cooled to 0° C. Diisopropylethylamine (3.1 mL, 18 mmol) followed by cyclopropylamine (3.0 mL, 43 mmol) was added and the mixture was allowed to warm up to RT and stirred for 1 hour. The mixture was concentrated and the crude product was purified by silica gel chromatography (50-100% EtOAc in hexanes) to give 610 mg of 3-(1-chlorophthalazin-6-yl)-N-cyclopropyl-4-methylbenzamide as an off-white solid. MS (ES+)=338.1 (M+H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07759337B2
Source datasetuspto-grants-2010_07
ORD IDord-fd7c1be592e749c39cdd81026342ad77
Source noteuspto-grants-2010_07