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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 449486Erstellt: 24. Oktober 2026

Diisopropylethylamine → methyl (2S)-2-({[2-amino-4-(4-methylpiperazin-1-yl)quinazolin-7-yl]carbonyl}amino)-3-biphenyl-4-ylpropanoate

https://huagongshe.com/de/reaction/449486

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktDiisopropylethylamineHCID 81531—
EduktMethanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
Edukt(S)-Methyl 3-([1,1'-biphenyl]-4-yl)-2-aminopropanoateHCID 15714801—
Edukt2-Amino-4-(4-methylpiperazin-1-yl)quinazoline-7-carboxylic acidHCID 59496649—
LösungsmittelDimethylformamideHCID 6228—
Produktmethyl (2S)-2-({[2-amino-4-(4-methylpiperazin-1-yl)quinazolin-7-yl]carbonyl}amino)-3-biphenyl-4-ylpropanoateHCID 4977903813,6%

Reaktionsschritte

N,N,N′,N′-Tetramethyl-O-(7-azabenzotriazol-1-yl)uronium hexafluorophosphate (42 mg, 0.11 mmol) was added to a solution of 2-amino-4-(4-methylpiperazin-1-yl)quinazoline-7-carboxylic acid (20 mg, 0.07 mmol) in N,N-dimethylformamide (2 mL) and N,N-diisopropylethylamine (24 uL, 0.14 mmol). The methyl (2S)-2-amino-3-biphenyl-4-ylpropanoate (36 mg, 0.14 mmol) was added. The reaction was stirred for 2 h. at r.t., and was purified by RP-HPLC (pH=2) to afford the desired product (5 mg, 10%) as a white solid TFA salt. Analytical LCMS (M+H)+: m/z=525.1.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08481732B2
Quelldatensatzuspto-grants-2013_07
ORD IDord-51148be0f5ee4680ae5583e36fb1948b
Quellennotizuspto-grants-2013_07