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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1518342Erstellt: 26. Oktober 2026

4-Morpholinophenol → 2-[8-(Benzothiazol-2-ylcarbamoyl)-3,4-dihydro-1H-isoquinolin-2-yl]-5-[3-(4-morpholin-4-yl-phenoxy)-propyl]-thiazole-4-carboxylic acid

https://huagongshe.com/reaction/1518342

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-MorpholinophenolHCID 80510—
Edukt2-[8-(Benzothiazol-2-ylcarbamoyl)-3,4-dihydro-1H-isoquinolin-2-yl]-5-{3-[4-(4-cyano-thiophen-3-yl)-phenoxy]-propyl]-thiazole-4-carboxylic acidHCID 46836245—
Produkt2-[8-(Benzothiazol-2-ylcarbamoyl)-3,4-dihydro-1H-isoquinolin-2-yl]-5-[3-(4-morpholin-4-yl-phenoxy)-propyl]-thiazole-4-carboxylic acidHCID 46836369—

Reaktionsschritte

The title compound was prepared in a similar manner to the synthesis of compound 51 by substituting compound 51A with 4-morpholinophenol in step 2 of Example 51: 1H NMR (DMSO-d6): δ 7.96 (d, J=7.67 Hz, 1H), 7.72 (d, J=7.98 Hz, 1H), 7.60 (d, J=7.06 Hz, 1H), 7.27-7.42 (m, 4H), 6.88 (d, J=8.9 Hz, 2H), 6.75-6.79 (m, 2H), 4.76 (s, 2H), 3.85 (t, J=6.29 Hz, 2H), 3.64-3.68 (m, 6H), 3.07-3.11 (m, 2H), 2.95-2.98 (m, 6H), 1.87-1.94 (m, 2H). ESI (+)/MS: 656 (M+H)+.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08232273B2
Quelldatensatzuspto-grants-2012_07
ORD IDord-9125beac15ba49768def823e22e9a21d
Quellennotizuspto-grants-2012_07