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HRID 40683作成日:2026年10月24日

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

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

反応式

関与物質

役割名称HCID仕込み量
反応物Acetyl chlorideHCID 6367—
反応物DiisopropylethylamineHCID 81531—
反応物5-(8-Aminoisoquinolin-3-ylamino)pyrazine-2-carbonitrileHCID 44204558—
溶媒1,2-DichloroethaneHCID 11—
生成物N-(3-(5-cyanopyrazin-2-ylamino)isoquinolin-8-yl)acetamideHCID 4420455932%

反応手順

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).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530468B2
出典データセットuspto-grants-2013_09
ORD IDord-ac3b96b0049f4acba0cc8a0b36463c4e
出典メモuspto-grants-2013_09