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HRID 2109719作成日:2026年10月25日

Dimethylformamide → Tert-butyl 5-(phthalazin-6-yl)thiazol-2-ylcarbamate

https://huagongshe.com/reaction/2109719

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Cesium fluorideHCID 25953—
反応物6-BromophthalazineHCID 610436—
反応物tert-butyl N-(5-(tributylstannyl)-1,3-thiazol-2-yl)carbamateHCID 2763269—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
触媒HCID 178418397HCID 178418397—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物Tert-butyl 5-(phthalazin-6-yl)thiazol-2-ylcarbamateHCID 5763394076%

反応条件

温度100 °C

反応手順

A glass microwave reaction vessel was charged with 6-bromophthalazine (1.0 g, 5 mmol), tert-butyl 5-(tributylstannyl)thiazol-2-ylcarbamate (4.0 g, 7 mmol), DMF (4 mL), cesium fluoride (1.0 g, 10 mmol), copper(I) iodide (0.2 g, 1.0 mmol), and tetrakis(triphenylphosphine)palladium(0) (0.3 g, 0.2 mmol). The reaction mixture was stirred and heated at 100° C. overnight. The mixture was diluted with DCM (20 mL) and water (5 mL) and filtered through Celite. The organic solution was evaporated under reduced pressure, and the residue was adsorbed onto a plug of silica gel and chromatographed through a Redi-Sep pre-packed silica gel column (40 g), eluting with a gradient of 5% to 10% MeOH in DCM to provide the title compound (1.19 g, 76%). LCMS (M+H+) 329.3 calc. for C16H16N4O2S 329.3; 1H NMR (400 MHz, CDCl3) δ ppm 9.50 (s, J=13.69 Hz 1H), 9.46 (s, 1H), 8.01 (d, J=1.37, Hz 1H), 7.92 (d, J=8.41 Hz, 1H), 7.81 (s, 1H), 7.58 (s, 1H) 1.40 (s, 9H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07514566B2
出典データセットuspto-grants-2009_04
ORD IDord-c041daf27ee44c2ba9d964a257df7e37
出典メモuspto-grants-2009_04