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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1827161Generated: October 30, 2026

3,4,5-Trichloropyridazine → 4-[(5,6-Dichloro-pyridazin-4-ylamino)-methyl]-piperidine-1-carboxylic acid benzyl ester

https://huagongshe.com/reaction/1827161

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3,4,5-TrichloropyridazineHCID 70111—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Aminomethyl-1-N-Cbz-piperidineHCID 21955499—
SolventIsopropanolHCID 3776—
Product4-[(5,6-Dichloro-pyridazin-4-ylamino)-methyl]-piperidine-1-carboxylic acid benzyl esterHCID 10135291—

Reaction Steps

To a stirred solution of 3,4,5-trichloropyridazine (2.22 g, 12.08 mmol) and DIPEA (4.21 mL, 24.16 mmol) in IPA (25 mL) was added benzyl-4-(aminomethyl)piperidine-1-carboxylate (EXAMPLE 13, Step 1, 3.00 g, 12.08 mmol). The resulting reaction solution was stirred at rt for 5 h, then concentrated in vacuo. The residue was dissolved in CH2Cl2 (200 mL), washed with water (50 mL), dried over Na2SO4, filtered and concentrated. The crude product was purified by silica gel chromatography (1-7 (10% NH4OH in MeOH)/99-93 CH2Cl2) to give 4-[(5,6-dichloro-pyridazin-4-ylamino)-methyl]-piperidine-1-carboxylic acid benzyl ester. M.S.(M+1):395.28

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07053089B2
Source datasetuspto-grants-2006_05
ORD IDord-ea04b501e9d14789815c27a8136fa85f
Source noteuspto-grants-2006_05