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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1806235Erstellt: 26. Oktober 2026

Dihydroxybenzylamine → 5-[3-({[(3,4-dihydroxyphenyl)methyl]amino}methyl)phenyl]-3-[1-(ethylsulfonyl)-4-piperidinyl]-1H-indole-7-carboxamide

https://huagongshe.com/reaction/1806235

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDihydroxybenzylamineHCID 91623—
EduktSodium triacetoxyborohydrideHCID 5049666—
Edukt3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-formylphenyl)-1H-indole-7-carboxamideHCID 57732804—
Lösungsmittel1,1-DichloroethaneHCID 6365—
Produkt5-[3-({[(3,4-dihydroxyphenyl)methyl]amino}methyl)phenyl]-3-[1-(ethylsulfonyl)-4-piperidinyl]-1H-indole-7-carboxamideHCID 1603820315,1%

Reaktionsschritte

To a solution of 3-[1-(ethylsulfonyl)-4-piperidinyl]-5-(3-formylphenyl)-1H-indole-7-carboxamide (50 mg, 0.114 mmol) in dichloroethane (2 mL) was added 4-(aminomethyl)-1,2-benzenediol (12.1 mg, 0.087 mmol). The reaction solution was stirred at ambient temperature for 10 min prior to addition of NaBH(OAc)3 (58 mg, 0.261 mmol). The resulting mixture was shaken overnight at ambient temperature after which time the solvent was removed under reduced pressure. The crude product was purified by reverse phase HPLC (water/CH3CN, 0.1% TFA 10-90%) to give the title compound (7.4 mg, 12%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08354406B2
Quelldatensatzuspto-grants-2013_01
ORD IDord-16a06a40570c43ab95fa819c4bcc2391
Quellennotizuspto-grants-2013_01