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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 514393Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/514393

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 4-(4-methylphenyl)-2,4-dioxobutanoateHCID 308119—
Edukt2-Hydrazinylpyridine-4-carbonitrile hydrochloride saltHCID 86725484—
LösungsmittelAcetic AcidHCID 176—
Produktmethyl 1-(4-cyanopyridin-2-yl)-5-(4-methylphenyl)-1H-pyrazole-3-carboxylateHCID 8672551985%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09107916B2
Quelldatensatzuspto-grants-2015_08
ORD IDord-9200489db5bb4663af329ed15a58889a
Quellennotizuspto-grants-2015_08