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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1486750Generated: October 26, 2026

1,2-Dichloroethane → HCID 118521865, compound

https://huagongshe.com/reaction/1486750

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DichloroethaneHCID 11—
Reactant3-Chloro-6-methylpyridazine-4-carboxylic acidHCID 26599215—
Reactant1-(3-Amino-benzyl)-piperidine-4-carboxylic acid tert-butylamideHCID 86706525—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 118521865HCID 118521865—

Reaction Steps

A solution of 1-(3-amino-benzyl)-piperidine-4-carboxylic acid tert-butylamide BB-4 (400 mg, 1.4 mmol) in DCM (15 mL) is treated successively with 3-chloro-6-methyl-pyridazine-4-carboxylic acid (239 mg, 1.4 mmol), EDC (344 mg, 1.8 mmol) and DMAP (25.3 mg, 0.207 mmol) at RT overnight. The reaction mixture is washed twice with sat.aq. NaHCO3 (15 mL). The aqueous phase is extracted twice with DCM (2×10 mL). The combined organic layers are dried over MgSO4 and filtered. The solvent is evaporated under reduced pressure. The residue is purified by prep HPLC E delivering the title compound (53 mg, 36%) as a light brownish powder, LC-MS A: tR=0.60 min; [M+H]+=444.12.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09428456B2
Source datasetuspto-grants-2016_08
ORD IDord-7954e4882bd14dbc9cc23f7fd0fa971a
Source noteuspto-grants-2016_08