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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1157237Generated: November 1, 2026

Hydrochloric Acid → 6-(4-amino-2,6-dichloro-benzyl)-4-isopropyl-2H-pyridazin-3-one

https://huagongshe.com/reaction/1157237

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantWaterHCID 962—
ReactantSodium HydroxideHCID 14798—
Reactant(4-Amino-2,6-dichloro-phenyl)-(6-chloro-5-isopropyl-pyridazin-3-yl)-acetonitrileHCID 59834538—
SolventAcetic AcidHCID 176—
Product6-(4-amino-2,6-dichloro-benzyl)-4-isopropyl-2H-pyridazin-3-oneHCID 5983444976%

Reaction Conditions

Temperature120 °C

Reaction Steps

A mixture of (4-amino-2,6-dichloro-phenyl)-(6-chloro-5-isopropyl-pyridazin-3-yl)-acetonitrile (45) (6.98 g, 19.63 mmol), water (30 mL), concentrated hydrochloric acid (120 mL) and glacial acetic acid (30 mL) was heated to 120° C. for 24 h. At this time, the reaction was cooled to room temperature and the mixture was poured onto water (250 mL). The pH was made neutral (pH=7) by the addition of a 4N aqueous sodium hydroxide solution. The suspension was placed in the freezer for 15 min. The resulting solids were filtered and washed with water and petroleum ether. The solids were collected and dissolved in hot ethyl acetate. Silica gel 60 (70-230 mesh) was added and the solvent was concentrated under vacuum. The resulting mixture was purified by flash chromatography (Biotage 75S) using silica gel eluted with 40% ethyl acetate in hexanes to 50% ethyl acetate in hexanes containing 0.5% glacial acetic acid. The desired fractions were collected and concentrated under vacuum to afford a solid which was dried under high vacuum to afford 6-(4-amino-2,6-dichloro-benzyl)-4-isopropyl-pyridazin-3-one (46) (4.65 g, 76%) as an off-white solid; LRMS for C14H15Cl2N3O (M+H) m/z=312. Molecular Weight=312.2012; Exact Mass=311.0592

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07807674B2
Source datasetuspto-grants-2010_10
ORD IDord-1db641172e4e441e8a4839707f7d85a0
Source noteuspto-grants-2010_10