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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2046255Generated: October 30, 2026

Hydrochloric Acid → HCID 57893420, compound

https://huagongshe.com/reaction/2046255

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantDimethylformamideHCID 6228—
ReactantSodium hydrideHCID 24758—
Reactant1-(Bromomethyl)-4-(1,1-dimethylethyl)benzeneHCID 87836—
ReactantHCID 54693618HCID 54693618—
ReactantHCID 68811893HCID 68811893—
ProductHCID 57893420HCID 5789342056%

Reaction Steps

Ethyl 6-cyclohexyl-2-{[4-(1,1-dimethylethyl)phenyl]methyl}-5-hydroxy-3-oxo-2,3-dihydro-4-pyridazinecarboxylate. Sodium hydride (0.040 g of a 60% oil suspension, 1.00 mmol) was added to a stirred suspension of ethyl 6-cyclohexyl-5-hydroxy-3-oxo-2,3-dihydro-4-pyridazinecarboxylate (example 10(a), 0.100 g, 0.376 mmol) in dimethylformamide (2.0 mL) under nitrogen. After 15 min stirring at room temperature, the mixture was cooled in an ice bath and 4-tert-butylbenzyl bromide (0.071 mL, 0.384 mmol) injected. The mixture was stirred for 0.5 h at 0° C. and 3 h at room temperature. 0.1M aqueous hydrochloric acid (50 mL) was added and the mixture extracted with ethyl acetate. The extracts were washed with dilute aqueous sodium chloride, then dried (MgSO4), evaporated under reduced pressure and the residue chromatographed (silica gel, 0-6% methanol/dichloromethane) to give the title compound (0.087 g, 56%) as a gum. LCMS (ES+) m/z 413 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE044613E1
Source datasetuspto-grants-2013_11
ORD IDord-175a439f0bb94d03a465f88e8b555e31
Source noteuspto-grants-2013_11