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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 570637Erstellt: 25. Oktober 2026

Diisopropylethylamine → Propyl [7-(4-benzyl-1H-1,2,3-triazol-1-yl)-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl]acetate

https://huagongshe.com/reaction/570637

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktBenzylacetyleneHCID 575753—
EduktPropyl (7-azido-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl)acetateHCID 59487226—
KatalysatorCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
LösungsmittelTetrahydrofuranHCID 8028—
ProduktPropyl [7-(4-benzyl-1H-1,2,3-triazol-1-yl)-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl]acetateHCID 86645391—

Reaktionsschritte

To a stirred solution of propyl (7-azido-6,7,8,9-tetrahydropyrido[1,2-α]indol-10-yl)acetate (1 eq) (Synthesis described in WO07019675 A1) and prop-2-yn-1-ylbenzene (2 eq) in tetrahydrofuran (THF) (0.1M) at room temperature was added diisopropyl ethylamine (DIPEA) (5 eq) and CuI (5 eq). The reaction mixture was stirred overnight then quenched with NH4Cl sat and extracted with ethyl acetate (EA), washed with brine, dried over Na2SO4 and evaporated. Purification by combi-flash EA/Hex 0-100% afforded the desired compound which was used directly for next step.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS09023864B2
Quelldatensatzuspto-grants-2015_05
ORD IDord-3916992b22c845a7bf20a3466f4db58c
Quellennotizuspto-grants-2015_05