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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1640287Erstellt: 26. Oktober 2026

N-Ethylbenzylamine → N-benzyl-N-ethyl-6-(2'-oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-5-yl-amino)pyrimidine-4-carboxamide

https://huagongshe.com/reaction/1640287

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktN-EthylbenzylamineHCID 84352—
EduktO-(Benzotriazol-1-yl)-N,N,N',N'-tetramethyluronium tetrafluoroborateHCID 2733207—
Edukt6-(2'-Oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-5-yl-amino)pyrimidine-4-carboxylic acid-hydrochlorideHCID 66722185—
LösungsmittelDimethylformamideHCID 6228—
ProduktN-benzyl-N-ethyl-6-(2'-oxo-1,1',2',3-tetrahydrospiro[indene-2,3'-pyrrolo[2,3-b]pyridin]-5-yl-amino)pyrimidine-4-carboxamideHCID 49801374—

Reaktionsschritte

100 mg (0.24 mmol) 6-(2′-oxo-1,1′,2′,3-tetrahydrospiro[indene-2,3′-pyrrolo[2,3-b]pyridin]-5-ylamino)pyrimidine-4-carboxylic acid hydrochloride, 50 μL (0.33 mmol) benzyl-ethyl-amine, 0.10 mL (0.72 mmol) TEA and 85 mg (0.27 mmol) TBTU in 1.8 mL DMF were stirred overnight at RT. The purification was carried out by preparative HPLC-MS. The product-containing fractions were combined and lyophilised.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08110575B2
Quelldatensatzuspto-grants-2012_02
ORD IDord-6564e9956e884df2ad29614950053b8c
Quellennotizuspto-grants-2012_02