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HRID 419068Erstellt: 25. Oktober 2026

Diisopropylethylamine → 1,2,3,4-Tetrahydro-1,8-naphthyridine

https://huagongshe.com/reaction/419068

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
Edukt1,8-NaphthyridineHCID 136069—
EduktBenzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
Edukt1,2,3,4-Tetrahydro-1,8-naphthyridineHCID 13047367—
Edukt5-Chloro-3-(4-chloro-3-trifluoromethyl benzenesulfonylamino)-pyridine-2-carboxylic acidHCID 57942077—
Produkt1,2,3,4-Tetrahydro-1,8-naphthyridineHCID 13047367—
Produkt4-chloro-N-[5-chloro-2-(3,4-dihydro-2H-[1,8]naphthyridine-1-carbonyl)-pyridin-3-yl]-3-trifluoromethyl-benzenesulfonamideHCID 57942323—

Reaktionsschritte

5-Chloro-3-(4-chloro-3-(trifluoromethyl)phenylsulfonamido)picolinic acid (208 mg, 0.50 mmol), 1,2,3,4-tetrahydro-[1,8]naphthyridine [(135 mg, 1.0 mmol) 1,2,3,4-tetrahydro-[1,8]naphthyridine was prepared freshly from 1,8-napthyridine via hydrogenation over Pt2O], BOP (486 mg, 1.1 mmol), DIEA (185 mg, 1.4 mmol) were reacted according to the procedure D to provide the title compound. HPLC purification (20→90% gradient of MeCN-water) provided 4-chloro-N-[5-chloro-2-(3,4-dihydro-2H-[1,8]naphthyridine-1-carbonyl)-pyridin-3-yl]-3-trifluoromethyl-benzenesulfonamide: MS m/z: 531.0 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08093247B2
Quelldatensatzuspto-grants-2012_01
ORD IDord-9696dc3f1b6b40a9912ee1c1b98ad082
Quellennotizuspto-grants-2012_01