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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 17242Erstellt: 24. Oktober 2026

Hydrochloric Acid → 2-[4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridin-7-yl]cyclopropanecarboxylic acid

https://huagongshe.com/de/reaction/17242

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktSodium HydroxideHCID 14798—
Eduktethyl 2-[4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridin-7-yl]cyclopropanecarboxylateHCID 18450882—
LösungsmittelMethanolHCID 887—
Produkt2-[4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridin-7-yl]cyclopropanecarboxylic acidHCID 1845055014,8%

Reaktionsschritte

Ethyl 2-[4-amino-3-(3-methoxy-4-{[(1-methyl-1H-indol-2-yl)carbonyl]amino}phenyl)thieno[3,2-c]pyridin-7-yl]cyclopropanecarboxylate (433 mg, 0.8018 mmol) in methanol (2 mL) and 2M sodium hydroxide (1.604 mL, 3.207 mmol) was stirred for 23 hours at 50° C., cooled to room temperature and acidified to a pH of 4 with 1M hydrochloric acid. Solids were filtered off and washed with water. The material was purified by HPLC preparative to furnish the title compound as a white solid (61 mg 0.119 mmol): LCMS (Conditions a): MH30 =513 Rt=2.22 minutes; 1H NMR (DMSO-d6, 400 MHz) 9.51 (1 H), 7.99 (1 H), 7.71 (2 H), 7.57 (2 H), 7.34 (2 H), 7.19 (1 H), 7.15 (1 H), 7.07 (1 H), 5.46 (1 H), 4.04 (3 H), 3.91 (3 H), 2.39 (1 H), 1.73 (1 H), 1.46 (1 H), 1.39 (1 H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07737160B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-0a7089297df04bbb97bab492030c82dd
Quellennotizuspto-grants-2010_06