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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 219939Erstellt: 25. Oktober 2026

3-(Acetylamino)-4-(2-methylpiperidin-1-yl)benzoic acid → Methyl 4-{5-[3-(acetylamino)-4-(2-methylpiperidin-1-yl)phenyl]-1,2,4-oxadiazol-3-yl}-2-fluorobenzoate

https://huagongshe.com/reaction/219939

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt3-(Acetylamino)-4-(2-methylpiperidin-1-yl)benzoic acidHCID 59495824—
EduktMethyl 4-[amino(hydroxyimino)methyl]-2-fluorobenzoateHCID 76644654—
LösungsmittelMethanolHCID 887—
ProduktMethyl 4-{5-[3-(acetylamino)-4-(2-methylpiperidin-1-yl)phenyl]-1,2,4-oxadiazol-3-yl}-2-fluorobenzoateHCID 67528808—

Reaktionsschritte

The title compound was obtained following procedure described for example 4, step 1, but starting from Intermediate 1 (70 mg; 0.33 mmol) and Intermediate 32 (91.17 mg; 0.33 mmol). Title compound was isolated after trituration with MeOH as an off-white powder. 1H NMR (DMSO-d6, 300 MHz) δ 9.10 (bs, 1H), 8.88, (bs, 1H), 8.11 (t, J=7.6 Hz, 1H), 8.03 (dd, J=8.1, 1.5 Hz, 1H), 7.97-7.87 (m, 2H), 7.45 (d, 8.4 Hz, 1H), 3.90 (s, 3H), 3.19-3.12 (m, 1H), 2.96-2.89 (m, 1H), 2.65-2.57 (m, 1H), 2.19 (s, 3H), 1.87-1.66 (m, 4H), 1.53-1.44 (m, 2H), 0.84 (d, J=6 Hz, 3H). LC/MS (Method B): 453.3 (M+H)+. HPLC (Method A) Rt 5.16 min (purity: 97.5%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08202865B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-f0093e66595e42fea10571c1b8e55bf1
Quellennotizuspto-grants-2012_06