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HRID 541977Erstellt: 26. Oktober 2026

Isoxazole-5-carbonyl chloride → N-[6-Chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]-2-[(3S)-1-(isoxazol-5-ylcarbonyl)pyrrolidin-3-yl]acetamide bis(trifluoroacetate)

https://huagongshe.com/reaction/541977

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktIsoxazole-5-carbonyl chlorideHCID 2736707—
EduktN-[6-chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]-2-[(3S)-pyrrolidin-3-yl]acetamide tris(trifluoroacetate)HCID 86636313—
ProduktN-[6-Chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]-2-[(3S)-1-(isoxazol-5-ylcarbonyl)pyrrolidin-3-yl]acetamide bis(trifluoroacetate)HCID 8663632081%

Reaktionsschritte

The desired compound was prepared according to the procedure of Example D94 using N-[6-chloro-2,4,8,18,22-pentaazatetracyclo[14.3.1.1(3,7).1(9,13)]docosa-1(20),3(22),4,6,9(21),10,12,16,18-nonaen-12-yl]-2-[(3S)-pyrrolidin-3-yl]acetamide tris(trifluoroacetate) and isoxazole-5-carbonyl chloride as the starting materials in 81% yield. LCMS for C27H26ClN8O3 (M+H)+: m/z=545.0.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08871753B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-1389ea46e5854f4fa6ac85757dfbc368
Quellennotizuspto-grants-2014_10