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HRID 16735Erstellt: 25. Oktober 2026

Methyl 4-(1H-pyrazol-1-yl)benzoate → HCID 178490048, Verbindung

https://huagongshe.com/reaction/16735

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 4-(1H-pyrazol-1-yl)benzoateHCID 972639—
EduktTrimethylaluminumHCID 16682925—
Edukt1-tert-butyl-3-(3-methoxyphenethyl)-1H-pyrazol-5-amineHCID 57453934—
LösungsmittelFormic AcidHCID 284—
LösungsmittelTolueneHCID 1140—
LösungsmittelDichloromethaneHCID 6344—
ProduktHCID 178490048HCID 178490048—

Reaktionsbedingungen

Temperatur82 °C

Reaktionsschritte

5-[2-(3-Methoxyphenyl)ethyl]-2-tert-butyl-pyrazol-3-amine (0.2 g, 0.73 mmol) was dissolved in toluene (10 ml) and to this was added methyl 4-pyrazol-1-ylbenzoate (177 mg, 0.88 mmol) and AlMe3 (0.93 ml, 1.8 mmol). The reaction mixture was stirred overnight. The reaction mixture was diluted with DCM (15 ml), quenched with damp sodium sulfite and further stirred for 20 mins before being filtered. The solvent was removed in vacuo to yield a yellow gum. This gum was dissolved in formic acid (12 ml) and heated at 82° C. overnight. The reaction mixture was evaporated to dryness and the resulting product was passed through a SCX column, eluting initially with methanol followed by 2N ammonia/methanol. After solvent removal, a yellow solid was obtained which was triturated with hot acetonitrile to afford a white solid. The solid was filtered and dried (155 mg, 55%); 1H NMR (400.132 MHz, DMSO) δ 2.92 (s, 4H), 3.74 (s, 3H), 6.48 (s, 1H), 6.60 (s, 1H), 6.77 (d, 1H), 6.84-6.82 (m, 2H), 7.20 (t, 1H), 7.81 (s, 1H), 7.96 (d, 2H), 8.14 (d, 2H), 8.63 (s, 1H), 10.69 (s, 1H), 12.18 (s, 1H); MS: m/z 388 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737149B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-dc8d6fc880db41ba83d41c5493bff1ee
Quellennotizuspto-grants-2010_06