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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 40683Erstellt: 24. Oktober 2026

Acetyl chloride → N-(3-(5-cyanopyrazin-2-ylamino)isoquinolin-8-yl)acetamide

https://huagongshe.com/de/reaction/40683

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAcetyl chlorideHCID 6367—
EduktDiisopropylethylamineHCID 81531—
Edukt5-(8-Aminoisoquinolin-3-ylamino)pyrazine-2-carbonitrileHCID 44204558—
Lösungsmittel1,2-DichloroethaneHCID 11—
ProduktN-(3-(5-cyanopyrazin-2-ylamino)isoquinolin-8-yl)acetamideHCID 4420455932%

Reaktionsschritte

Acetyl chloride (13 mg, 0.16 mmol) was added to a solution of 5-(8-aminoisoquinolin-3-ylamino)pyrazine-2-carbonitrile (36 mg, 0.14 mmol) and diisopropylethylamine (39 mg, 0.30 mmol) in DCE (1.5 mL). The reaction mixture stirred at room temperature for 16 hours and another portion of acetyl chloride (6.5 mg, 0.08 mmol) was added. Stirring was continued for a further 24 hours. The reaction mixture was washed once with water and the organic phase was dried (Na2SO4) and concentrated to dryness. Preparative HPLC gave N-(3-(5-cyanopyrazin-2-ylamino)isoquinolin-8-yl)acetamide (13.4 mg, 0.044 mmol, 32%). 1H NMR (d6-DMSO, 400 MHz) δ 11.05 (br s, 1H), 10.20 (s, 1H), 9.36 (s, 1H), 8.82 (d, 1H, J=1.2 Hz), 8.72 (d, 1H, J=1.2 Hz), 8.48 (s, 1H), 7.65-7.75 (m, 3H), 2.22 (s, 3H). LC-MS (2) Rt=1.96 min; m/z (ESI+) 305 (M+H).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS08530468B2
Quelldatensatzuspto-grants-2013_09
ORD IDord-ac3b96b0049f4acba0cc8a0b36463c4e
Quellennotizuspto-grants-2013_09