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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056446Generated: October 26, 2026

5-Chloro-2-(trifluoromethyl)benzoyl chloride → 6-[4-(5-CHLORO-2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZINE-3-CARBOXYLIC Acid (3-METHYLBUTYL)AMIDE

https://huagongshe.com/reaction/2056446

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-Chloro-2-(trifluoromethyl)benzoyl chlorideHCID 2778107—
Reactant6-Piperazin-1-yl-pyridazin-3-carboxylic acid (3-methylbutyl)amideHCID 66849322—
Product6-[4-(5-CHLORO-2-TRIFLUOROMETHYLBENZOYL)PIPERAZIN-1-YL]PYRIDAZINE-3-CARBOXYLIC Acid (3-METHYLBUTYL)AMIDEHCID 86597215—

Reaction Steps

Following the procedure of Example 3, making variations only as required to use 5-chloro-2-trifluoromethylbenzoyl chloride in place of isoxazole-5-carbonyl chloride to react with 6-piperazin-1-yl-pyridazine-3-carboxylic acid (3-methylbutyl)amide, the title compound was obtained as a white solid (80%). m.p. 148-151° C. 1H NMR (400 MHz, CDCl3) δ 8.06, 7.85, 7.67, 7.54-7.50, 7.35, 7.01, 4.05-3.34, 1.73-1.46, 0.98. MS (ES+) m/z 484.3 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335658B2
Source datasetuspto-grants-2008_02
ORD IDord-eddc67384fc34f6185d5eabd606db8be
Source noteuspto-grants-2008_02