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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2168714Generated: November 2, 2026

Hydrochloric Acid → HCID 67371488, compound

https://huagongshe.com/reaction/2168714

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDiethyl EtherHCID 3283—
ReactantHCID 67373525HCID 67373525—
SolventDichloromethaneHCID 6344—
ProductHCID 67371488HCID 67371488—

Reaction Steps

To a solution of 3-cyclohexyl-4-(4-cyclohexyloxy-phenyl)-6-(piperidin-4-yloxy)-pyridazine dihydrochloride (0.079 mmol, 0.04 g) and aqueous formaldehyde (37%, 0.39 mmol, 0.035 mL) in dry DCM (1 mL) was added macroporous resin-bound triacetoxyborohydride (loading 2.36 mmol/gram, 0.47 mmol, 0.20 g). The mixture was shaken for 2 hours. The reaction was placed directly onto a 4 g SiO2 cartridge and the column was eluted with 4-6% (2N NH3 in MeOH) in DCM to give 3-cyclohexyl-4-(4-cyclohexyloxy-phenyl)-6-(1-methyl-piperidin-4-yloxy)-pyridazine. The neutral amine was treated with 2N HCl in diethyl ether (0.5 mL) and DCM (0.5 mL). The volatiles were removed under reduced pressure and the salt was triturated with diethyl ether and filtered to provide the title compound (0.04 g). LCMS: m/z 451 [M+1]. 1H NMR (400 MHz, CD3OD) δ 7.63-7.79 (1 H, m), 7.38-7.43 (2 H, m), 7.10-7.14 (2 H, m), 5.33-5.57 (1 H, m), 4.40-4.51 (1 H, m), 3.66-3.69 (1 H, m), 3.11-3.54 (3 H, m), 2.94 (3 H, s), 2.37-2.62 (2 H, m), 2.20-2.30 (1 H, m), 1.20-2.17 (22 H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09045461B2
Source datasetuspto-grants-2015_06
ORD IDord-004b0112c9b841509ecea5d2eacc29ab
Source noteuspto-grants-2015_06