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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2056536Generated: October 30, 2026

2,5-Dichlorobenzyl chloride → HCID 67011278, compound

https://huagongshe.com/reaction/2056536

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,5-Dichlorobenzyl chlorideHCID 75976—
ReactantN-(2-cyclopropylethyl)-6-(1-piperazinyl)-3-pyridazinecarboxamideHCID 66849327—
ProductHCID 67011278HCID 67011278—

Reaction Steps

Following the procedure of Example 11, making variations only as required to use 2,5-dichlorobenzyl chloride in place of 2-trifluoromethylbenzyl chloride to react with 6-piperazin-1-yl-pyridazine-3-carboxylic acid (2-cyclopropylethyl)amide, the title compound was obtained as a white solid (43% yield). 1H NMR (300 MHz, CDCl3) δ 7.96-8.04, 7.53, 7.16-7.33, 6.96, 3.75-3.84, 3.64, 3.56, 2.62-2.70, 1.53, 1.51, 0.70-0.83, 0.43-0.51, 0.06-0.13. MS (ES+) m/z 434 (M).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07335658B2
Source datasetuspto-grants-2008_02
ORD IDord-5c5f7002600d42c1a491d8a3c5df8e6b
Source noteuspto-grants-2008_02