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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168697Generated: October 29, 2026

Hydrochloric Acid → HCID 67373738, compound

https://huagongshe.com/reaction/2168697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantAcetyl chlorideHCID 6367—
ReactantDiisopropylethylamineHCID 81531—
ReactantHCID 67373335HCID 67373335—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
ProductHCID 67373738HCID 67373738—

Reaction Steps

To a solution of 3-butyl-6-(1-methyl-piperidin-4-yloxy)-4-[4-(piperidin-4-ylmethoxy)-phenyl]-pyridazine dihydrochloride (0.2 mmol, 103 mg) in DCM (1 mL) at 0° C. was added acetyl chloride (0.4 mmol, 29 μL), DIEA (0.4 mmol, 70 μL) and DMAP (5 mg). The mixture was stirred at room temperature for 1 hour. The mixture was then condensed in vacuo and the residue was purified by silica gel chromatography (DCM to DCM+10% 2N NH3 in MeOH) to give a colorless sticky solid, which was dissolved in DCM (1.0 mL), 2N HCl in ether (1.0 mL) was added, kept at room temperature for 10 min, condensed, triturated with hexanes to provide the title compound. LCMS: m/z 482 [M+1]. 1H NMR (400 MHz, CD3OD): δ 7.63 and 7.75 (1 H, s), 7.44-7.50 (2 H, m), 7.12-7.17 (2 H, m), 5.37-5.54 (1 H, m), 4.37 (2 H, d), 3.36-3.69 (3 H, m), 3.08-3.30 (4 H, m), 2.92 (3 H, s), 2.11-2.74 (5 H, m), 2.10 (3 H, s), 1.86-2.08 (4 H, m), 1.25-1.54 (7 H, m), 0.82 (3 H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045461B2
Source datasetuspto-grants-2015_06
ORD IDord-fa3dee63ba974a7da19389c2768793b9
Source noteuspto-grants-2015_06