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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1429668Generated: October 25, 2026

Sodium Carbonate → N-[1-(4-chlorobenzyl)piperidin-4-yl]-6-chloropyridazin-3-amine

https://huagongshe.com/reaction/1429668

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant3,6-DichloropyridazineHCID 67331—
Reactant1-((4-Chlorophenyl)methyl)piperidin-4-amineHCID 7130833—
SolventWaterHCID 962—
SolventDimethylacetamideHCID 31374—
ProductN-[1-(4-chlorobenzyl)piperidin-4-yl]-6-chloropyridazin-3-amineHCID 59805852—

Reaction Conditions

Temperature120 °C

Reaction Steps

A solution of 1-(4-chlorobenzyl)-piperidin-4-yl amine (1 g, 4.45 mmol) (prepared by a procedure similar to that described in WO2001098273), 3,6-dichloropyridazine (670 mg, 4.45 mmol) and sodium carbonate (940 mg, 8.90 mmol) in dimethylacetamide (5 ml) was heated at 120° C. in a microwave reactor (Emrys Optimizer; 0-9 Barr) for 40 minutes. After this period, the reaction mixture was diluted with water and extracted with dichloromethane. The organic layer was dried (MgSO4), filtered and the solvents evaporated in vacuo. Purification by reverse phase HPLC (conditions as previously described) gave E16 (228 mg, 15%). C16H18Cl2N4 requires 336; Found 337 (MH+). 1H NMR (360 MHz, CDCl3) δ1.52 (qd, J=11.5, 3.5 Hz, 2H), 2.08 (d, J=12.5 Hz, 2H), 2.16 (t, J=11.3 Hz, 2H), 2.82 (d, J=11.5 Hz, 2H), 3.48 (s, 2H), 3.77-3.87 (m, 1H), 4.55 (d, J=7.8 Hz, 1H), 6.59 (d, J=9.3 Hz, 1H), 7.14 (d, J=9.3 Hz, 1H), 7.25 (d, J=7.7 Hz, 2H), 7.29 (d, J=7.7 Hz, 2H)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940743B2
Source datasetuspto-grants-2015_01
ORD IDord-be6bfbf89bd64deaadc901757fb7af05
Source noteuspto-grants-2015_01