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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 878551Generated: October 25, 2026

Methyl 4-(4-methylphenyl)-2,4-dioxobutanoate → methyl 1-(4-cyanopyridin-2-yl)-5-(4-methylphenyl)-1H-pyrazole-3-carboxylate

https://huagongshe.com/reaction/878551

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl 4-(4-methylphenyl)-2,4-dioxobutanoateHCID 308119—
Reactant2-Hydrazinylpyridine-4-carbonitrile hydrochloride saltHCID 86725484—
SolventAcetic AcidHCID 176—
Productmethyl 1-(4-cyanopyridin-2-yl)-5-(4-methylphenyl)-1H-pyrazole-3-carboxylateHCID 8672551985%

Reaction Steps

A solution of methyl 4-(4-methylphenyl)-2,4-dioxobutanoate (500 mg, 22.7 mmol) and 2-hydrazinylpyridine-4-carbonitrile hydrochloride salt (500 mg, 24.2 mmol, PREPARATION 3) in AcOH (10 mL) was heated at 100° C. for 30 min and cooled to rt. The solution was concentrated to an oily residue which was partitioned between EtOAc (50 mL) and water (50 mL). The pH was adjusted to pH=8 using a saturated aq. Na2CO3 solution. The organics were dried (MgSO4), filtered, and concentrated to give a solid which was triturated with MTBE/hexanes (1:1) and filtered to give the title compound (613 mg, 85%) as a yellow solid. 1H NMR (400 MHz, CD3OD): δ 2.48 (3H, s), 3.92 (3H, s), 7.01 (1H, s), 7.08-7.21 (4H, m), 7.71 (1H, d, J=4.8 Hz), 8.12 (1H, s), 8.48 (1H, d, J=4.8 Hz), 8.00 (1H, s), 8.48 (1H, d, J=8 Hz).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987461B2
Source datasetuspto-grants-2015_03
ORD IDord-53a64626dfae46b48e142051111f1f01
Source noteuspto-grants-2015_03