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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 888448Erstellt: 24. Oktober 2026

D-Camphorsulfonic Acid → HCID 69812522, Verbindung

https://huagongshe.com/de/reaction/888448

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktD-Camphorsulfonic AcidHCID 65617—
Edukt3,5-Dibromo-1-methyl-1H-pyrazin-2-oneHCID 13062969—
Edukt3-(4-Aminophenyl)-4-ethylpiperazin-2-oneHCID 57625167—
LösungsmittelIsopropanolHCID 3776—
ProduktHCID 69812522HCID 6981252279%

Reaktionsschritte

A 100-mL single-neck round-bottomed flask equipped with a magnetic stirrer and reflux condenser was charged with 33 (450 mg, 2.05 mmol), isopropanol (5 mL), 13 (603 mg, 2.26 mmol) and DL-10-camphorsulfonic acid (813 mg, 3.50 mmol), and the reaction mixture was then stirred at reflux for 16 h. After this time, the reaction mixture was cooled to room temperature, filtered and the filter cake washed with isopropanol (10 mL). The resulting solid was dissolved in methylene chloride/methanol (3:1), absorbed onto silica gel and purified by flash chromatography to afford 34 in 79% yield (654 mg) as an orange solid: mp 152-153° C.; 1H NMR (500 MHz, CDCl3) 8.28 (bs, 1H 7.73 (d, 2H, J=8.5 Hz), 7.43 (d, 2H, J=8.5 Hz), 6.74 (s, 1H), 5.90 (d, 1H, J=3.5 Hz), 4.12 (s, 1H), 3.60 (m, 1H), 3.52 (s, 3H), 3.36 (m, 1H), 3.12 (m, 1H), 2.60 (m, 2H), 2.28 (m, 1H), 1.00 (t, 3H, J=7.0 Hz); MS (ESI+) m/z 406.0 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08247550B2
Quelldatensatzuspto-grants-2012_08
ORD IDord-7578d5d25cc34485b5cdb7958ec3a929
Quellennotizuspto-grants-2012_08