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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1971889Generated: November 1, 2026

Hydrochloric Acid → HCID 67373987, compound

https://huagongshe.com/reaction/1971889

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantFormaldehydeHCID 712—
ReactantWaterHCID 962—
ReactantSodium triacetoxyborohydrideHCID 5049666—
ReactantHCID 67375265HCID 67375265—
CatalystAcetic AcidHCID 176—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
SolventWater ethylacetateHCID 22728543—
ProductHCID 67373987HCID 67373987154.6%

Reaction Steps

To a solution of 4-(4-benzyloxy-phenyl)-3-butyl-6-(pyrrolidin-3-ylmethoxy)-pyridazine dihydrochloride (0.3 mmol, 147 mg) in dichloromethane (2 mL) was added formaldehyde solution in water (37%, 10 mmol, 1.0 mL), and 2 drops of acetic acid. Then sodium triacetoxyborohydride (10 mmol, 2.12 g) was added. And the mixture was stirred at room temperature for 0.5 hour then condensed. It was then diluted with water/EtOAc and neutralized with NaHCO3 powder. The solvent was removed 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 (117 mg). LCMS: m/z 433 [M+1]. 1H NMR (400 MHz, CD3OD) δ 7.82 (1H, s), 7.45-7.55 (4H, m), 7.36-7.40 (2H, m), 7.31-7.35 (1H, m), 7.21-7.24 (2H, m), 5.20 (2H, s), 4.43 (2H, d), 3.57-3.62 (2H, m), 3.05-3.17 (3H, m), 2.87 (3H, s), 2.14-2.30 (2H, m), 1.70-1.81 (2H, m), 1.45-1.53 (2H, m), 1.23-1.33 (2H, m), 0.81 (3H, t).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08431575B2
Source datasetuspto-grants-2013_04
ORD IDord-384d97d1f6154a1a924c9be2950195d4
Source noteuspto-grants-2013_04