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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 535423Erstellt: 26. Oktober 2026

Methylamine → 2-(ethylamino)-N-[5-pyrimidin-5-yl-6-(2-quinolin-6-ylethynyl)pyridin-2-yl]butanamide

https://huagongshe.com/reaction/535423

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethylamineHCID 6329—
EduktDiisopropylethylamineHCID 81531—
Edukt2-Bromobutanoyl bromideHCID 117293—
Edukt5-Pyrimidin-5-yl-6-(2-quinolin-6-ylethynyl)pyridin-2-amineHCID 86694413—
LösungsmittelDichloromethaneHCID 6344—
LösungsmittelTetrahydrofuranHCID 8028—
LösungsmittelN-methyl-2-pyrrolidoneHCID 13387—
Produkt2-(ethylamino)-N-[5-pyrimidin-5-yl-6-(2-quinolin-6-ylethynyl)pyridin-2-yl]butanamideHCID 86694412—

Reaktionsschritte

5-pyrimidin-5-yl-6-(2-quinolin-6-ylethynyl)pyridin-2-amine G2b (600 mg, 1.86 mmol) is mixed with NMP (10 ml) and DIPEA (1.42 ml, 8.35 mmol). 2-Bromobutanoyl bromide (985 μl, 8.17 mmol) is added dropwise. The mixture stirred for 1 h at RT. The mixture is diluted with DCM and extracted with a saturated aqueous solution of NaHCO3. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The crude intermediate is mixed with a THF solution of methylamine (2 mol/l, 5 ml, 10 mmol) and stirred at RT for 16 h. The mixture is diluted with DCM and extracted with a saturated aqueous solution of NaHCO3. The combined organic layers are dried over MgSO4 and concentrated in vacuo. The product is purified by RP HPLC. Yield: 250 mg (32%). HPLC-MS: M+H=423; tR=1.25 min (*Method—1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08859541B2
Quelldatensatzuspto-grants-2014_10
ORD IDord-c2813ae979d3436c916f4e26cc601651
Quellennotizuspto-grants-2014_10