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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 49569Erstellt: 24. Oktober 2026

2,5-Dibromopyridine → Benzyl 3-(5-bromopyridin-2-yl)prop-2-ynylcarbamate

https://huagongshe.com/de/reaction/49569

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt2,5-DibromopyridineHCID 69353—
EduktBenzyl prop-2-yn-1-ylcarbamateHCID 11137906—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
KatalysatorHCID 178418476HCID 178418476—
LösungsmittelDiisopropylamineHCID 7912—
LösungsmittelEthyl AcetateHCID 8857—
ProduktBenzyl 3-(5-bromopyridin-2-yl)prop-2-ynylcarbamateHCID 2129938273,8%

Reaktionsschritte

A mixture of 2,5-dibromopyridine (1.19 g), N-Cbz-propargylamine (1.04 g), Pd(PPh3)2Cl2 (73 mg), and CuI (10 mg) in diisopropylamine (20 mL) was stirred at ambient temperature for 3 hours under nitrogen. The mixture was diluted with ethyl acetate (50 mL). The mixture was filtered and washed with ethyl acetate (20 mL). The filtrate and wash were combined, concentrated under reduced pressure and triturated in MTBE to give crystalline 7-1 (1.28 g). The mother liquor was further purified by silica gel column chromatography using a mixture of MTBE: hexanes (1:1) to give an additional 280 mg of 7-1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06706885B2
Quelldatensatzuspto-grants-2004_03
ORD IDord-26c2d7fafdc044be956e21bc0a6f0e9f
Quellennotizuspto-grants-2004_03