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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2097493Generated: November 2, 2026

Potassium Phosphate, Tribasic → 3-Methyl-1,5-bis(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one

https://huagongshe.com/reaction/2097493

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium Phosphate, TribasicHCID 62657—
ReactantMethylboronic AcidHCID 139377—
Reactant2-Dicyclohexylphosphino-2',6'-dimethoxybiphenylHCID 11269872—
Reactant3-Iodo-1,5-bis(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-oneHCID 66602504—
Catalystpalladium(II) acetateHCID 167845—
SolventTolueneHCID 1140—
SolventTetrahydrofuranHCID 8028—
Product3-Methyl-1,5-bis(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-oneHCID 66602502917.4%

Reaction Steps

1 ml of tetrahydrofuran was added to 34 mg (0.15 mmol) of palladium acetate and 126 mg (0.306 mmol) of 2-dicyclohexylphosphino-2′,6′-dimethoxybiphenyl, the mixture was degassed under reduced pressure and replaced with argon. Then, the mixture was stirred at room temperature for 30 minutes. Thereafter, 1.59 g (3.04 mmol) of 3-iodo-1,5-bis(2-trimethylsilylethoxymethyl)-1,5-dihydropyrrolo[2,3-d]pyridazin-4-one obtained in Reference example 18-(b), 551 mg (9.20 mmol) of methylboronic acid, 2.62 g (12.3 mmol) of potassium phosphate and 9 ml of toluene were added to the mixture, and after the resulting mixture was again degassed under reduced pressure and replaced with argon, the mixture was stirred at 100° C. for 4 hours. After completion of the reaction, water was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer after separation was washed with a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate and then concentrated under reduced pressure. The obtained residue was applied to silica gel column chromatography (Eluent; hexane:ethyl acetate=19:1→3:2 (V/V)), and the fractions containing the desired compound were concentrated under reduced pressure to obtain 1.15 g of the title compound as a yellowish solid. (Yield: 92%)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08450319B2
Source datasetuspto-grants-2013_05
ORD IDord-0000bdb1a74b490bb315dc283ff7dad1
Source noteuspto-grants-2013_05