Zurück
HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1984791Erstellt: 25. Oktober 2026

1,2-Dichloroethane → Benzyl 9-(5-{[(2-aminophenyl)amino]carbonyl}pyridin-2-yl)-3,9-diazaspiro[5.5]-undecane-3-carboxylate

https://huagongshe.com/reaction/1984791

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktO-PhenylenediamineHCID 7243—
EduktTriethylamineHCID 8471—
EduktBenzyl chloroformateHCID 10387—
Edukt1-HydroxybenzotriazoleHCID 75771—
EduktLithium hydroxide, monohydrateHCID 168937—
EduktTert-butyl 9-[5-(methoxycarbonyl)pyridin-2-yl]-3,9-diazaspiro[5.5]undecane-3-carboxylateHCID 57717452—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTrifluoroacetic acidHCID 6422—
LösungsmittelMethanol tetrahydrofuran waterHCID 21892291—
ProduktBenzyl 9-(5-{[(2-aminophenyl)amino]carbonyl}pyridin-2-yl)-3,9-diazaspiro[5.5]-undecane-3-carboxylateHCID 57717481—

Reaktionsschritte

A solution of tert-butyl 9-[5-(methoxycarbonyl)pyridin-2-yl]-3,9-diazaspiro[5.5]undecane-3-carboxylate (100 mg, 0.257 mmol) in 1 mL of CH2Cl2 and 1 mL of TFA was stirred for 1 h and concentrated. The oil was redissolved in 2 mL of CH2Cl2 and treated with NEt3 (0.15 mL, 1.08 mmol) and CbzCl (0.060 mL, 0.42 mmol), then stirred for 8 h. The mixture was partitioned between EtOAc and sat'd NaHCO3, dried (Na2SO4), filtered and concentrated. The residue was stirred in 3 mL of 1:1:1 MeOH/THF/water with LiOH.H2O (30 mg, 0.71 mmol) for 10 h, concentrated to dryness, dissolved in 2 mL of DMF, treated with EDC (150 mg, 0.79 mmol), HOBt (100 mg, 0.74 mmol), and phenylenediamine (100 mg, 0.93 mmol). The mixture was stirred for 18 h, concentrated, and triturated with methanol giving the title compound; MS (ESI+): cal'd [M+1]+ 500.3, obs'd 500.3.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07544695B2
Quelldatensatzuspto-grants-2009_06
ORD IDord-2ba8ca0ffb484d8687178a91911b37ca
Quellennotizuspto-grants-2009_06