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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 221978Erstellt: 23. Oktober 2026

1,2-Dichloroethane → HCID 58229894, Verbindung

https://huagongshe.com/de/reaction/221978

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1,2-DichloroethaneHCID 11—
EduktAcetic AcidHCID 176—
Edukt1-HydroxybenzotriazoleHCID 75771—
Edukt1-methyl-1H-imidazole-4-carboxylic acidHCID 541509—
EduktTert-butyl {2-[4-(5-hydrazino-3-phenyl-1,6-naphthyridin-2-yl)phenyl]-5,8-dioxaspiro[3.4]oct-2-yl}carbamateHCID 58229864—
LösungsmittelDimethylacetamideHCID 31374—
ProduktHCID 58229894HCID 58229894—

Reaktionsschritte

To a solution of 1-methyl-1H-imidazole-4-carboxylic acid (7.0 g, 56 mmol) in DMA (200 mL) was added EDC (11 g, 56 mmol) and HOBt (8.5 g, 56 mmol) and the reaction mixture was stirred at room temperature for 1 hour. Then tert-butyl {2-[4-(5-hydrazino-3-phenyl-1,6-naphthyridin-2-yl)phenyl]-5,8-dioxaspiro[3.4]oct-2-yl}carbamate (1-10) (30 g, 56 mmol) was added and the reaction stirred at room temperature for an additional 1 hour at which time acetic acid (17 g, 280 mmol) was added and the reaction was stirred overnight at 80° C., The reaction mixture was cooled to room temperature, quenched with 1N NaOH, poured into saturated sodium bicarbonate, extracted with EtOAc, dried (Na2SO4), filtered and concentrated. The crude residue was purified by column chromatography eluting with 10% methanol in DCM. The appropriate fractions were concentrated and the resulting solid was recrystallized from methanol to give tert-butyl (2-{4-[3-(1-methyl-1H-imidazol-4-yl)-9-phenyl[1,2,4]triazolo[3,4-f]-1,6-naphthyridin-8-yl]phenyl}-5,8-dioxaspiro[3.4]oct-2-yl)carbamate (1-11) as a white solid. MS (M+H)+: 630.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08207169B2
Quelldatensatzuspto-grants-2012_06
ORD IDord-b7cc9e988695408ead0fce38b95d045a
Quellennotizuspto-grants-2012_06