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HRID 1364114作成日:2026年10月25日

Pyridine → 1,1-Dimethylethyl 2-(4-cyanophenyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepine-6(2H)-carboxylate

https://huagongshe.com/reaction/1364114

反応式

関与物質

役割名称HCID仕込み量
反応物PyridineHCID 1049—
反応物4-Cyanophenylboronic acidHCID 2734326—
反応物HCID 178451637HCID 178451637—
触媒Cupric acetateHCID 8895—
溶媒DichloromethaneHCID 6344—
生成物1,1-Dimethylethyl 2-(4-cyanophenyl)-4,5,7,8-tetrahydropyrazolo[3,4-d]azepine-6(2H)-carboxylateHCID 66930765—

反応手順

1,1-Dimethylethyl 4,5,7,8-tetrahydropyrazolo[3,4-d]azepine-6(2H)-carboxylate (may be prepared as described in Description 9) (1.80 g, 7.58 mmol), 4-cyanophenyl boronic acid (2.23 g, 15.16 mmol; commercially available from e.g. Aldrich), copper(II) acetate (4.15 g, 22.76 mmol), pyridine (1.21 ml, 15.16 mmol) and powdered 4 Å molecular sieves (5.33 g) were stirred in dichloromethane (80 ml) at room temperature in air for 40 hours. The mixture was filtered through a pad of Kieselguhr and the filtrate evaporated. The residue was dissolved in ethyl acetate and the solution washed with 5% sodium bicarbonate solution (×3), dried over magnesium sulphate and evaporated. The residue was purified by flash chromatography eluting with 10-40% ethyl acetate in n-pentane to give the title compound (D10). MS (ES+) m/e 339 [M+H]+

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07888347B2
出典データセットuspto-grants-2011_02
ORD IDord-bf9f76de2df64c078bcf924e2d0db329
出典メモuspto-grants-2011_02