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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 384257Erstellt: 25. Oktober 2026

m-Aminoacetanilide → 2-(3-acetamidophenylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide

https://huagongshe.com/reaction/384257

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Eduktm-AminoacetanilideHCID 7604—
Eduktp-Toluenesulfonic acid monohydrateHCID 521998—
Edukt2-(1H-benzo[d][1,2,3]triazol-1-yloxy)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamideHCID 57472013—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt2-(3-acetamidophenylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamideHCID 5809891432,1%

Reaktionsbedingungen

Temperatur100 °C

Reaktionsschritte

To a solution of 2-(1H-benzo[d][1,2,3]triazol-1-yloxy)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide (60 mg, 0.15 mmol) in NMP (0.6 mL) was added 3-acetamidoaniline (25 mg, 0.165 mmol) and pTsOH.H2O (28 mg, 0.15 mmol). The mixture was heated at 100° C. for 2 h, cooled to room temperature, purified by preparative HPLC to give 2-(3-acetamidophenylamino)-4-(1-methyl-1H-indol-4-ylamino)pyrimidine-5-carboxamide (20 mg). MS found for C22H21N7O2 as (M+H)+ 416.3. λ=211.3, 250.9.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08367689B2
Quelldatensatzuspto-grants-2013_02
ORD IDord-36d1eb7dfce843bb91556a2c1b444a69
Quellennotizuspto-grants-2013_02