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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 15126Erstellt: 26. Oktober 2026

Water → (4R/S)-(3-chloro-4-hydroxy-7-oxo-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-4-yl)methyl 4-methylbenzenesulfonate

https://huagongshe.com/reaction/15126

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktWaterHCID 962—
Edukt4-Toluenesulfonyl chlorideHCID 7397—
EduktTriethylamineHCID 8471—
Edukt(4R/S)-3-Chloro-4-hydroxy-4-(hydroxymethyl)-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-oneHCID 23633411—
KatalysatorDibutyltin oxideHCID 61221—
Lösungsmitteldichloromethane tetrahydrofuran DMFHCID 86642945—
Produkt(4R/S)-(3-chloro-4-hydroxy-7-oxo-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-4-yl)methyl 4-methylbenzenesulfonateHCID 13172816495,2%

Reaktionsschritte

A suspension of (4R/S)-3-chloro-4-hydroxy-4-(hydroxymethyl)-4,5-dihydro-7H-pyrrolo[3,2,1-de]-1,5-naphthyridin-7-one (300 mg, 1.2 mmol) in dichloromethane/tetrahydrofuran/N,N-dimethylformamide (10 ml/10 ml/2 ml) was treated with triethylamine (0.25 ml, 1.8 mmol), para-toluenesulphonyl chloride (220 mg, 1.2 mol) and dibutyltin oxide (15 mg, 0.06 mmol). After 3 hours water was added and the phases separated. The organic phase was washed with saturated aqueous sodium bicarbonate solution then dried and evaporated affording the product (465 mg).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732460B2
Quelldatensatzuspto-grants-2010_06
ORD IDord-67728f421e3f4195ad806ed49d11f5d7
Quellennotizuspto-grants-2010_06