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HRID 1485579作成日:2026年10月27日

Potassium Carbonate → tert-Butyl (1-pyridazin-3-ylpiperidin-4-yl)carbamate

https://huagongshe.com/reaction/1485579

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物Cesium fluorideHCID 25953—
反応物4-(N-Boc-amino)piperidineHCID 723833—
反応物3-BromopyridazineHCID 13126699—
溶媒Dimethyl SulfoxideHCID 679—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
生成物tert-Butyl (1-pyridazin-3-ylpiperidin-4-yl)carbamateHCID 8662587135.4%

反応条件

温度100 °C

反応手順

The reaction mixture of tert-butyl piperidin-4-ylcarbamate (250 mg, 1.25 mmol), 3-bromopyridazine (258 mg, 1.62 mmol), CsF (37.9 mg, 0.25 mmol), and K2CO3 (518 mg, 3.74 mmol) in DMSO (12.5 mL) was heated at 100° C. for 20 h. Water and DCM were poured into the mixture, and the separated aqueous layer was extracted with DCM, the combined organic layers were dried over Na2SO4, filtered, concentrated in vacuo. The residue was purified by column chromatography (Hexane:EtOAc=1:1) to give tert-butyl 1-(pyridazine-3-yl)piperidin-4-ylcarbamate (123 mg, 35%) as a pale yellow solid. 1H-NMR (CDCl3, Varian 400 MHz) δ 1.45 (9H, s), 1.92-2.12 (2H, m), 3.03-3.17 (2H, m), 3.55-3.80 (2H, m), 4.25-4.38 (2H, m), 4.52 (1H, brs), 6.92 (1H, d, J=9.2 Hz), 7.20 (1H, dd, J=4.4, 9.2 Hz), 8.56 (1H, d, J=4.4 Hz). NH peak was not observed. m/z=279.06 [M+1]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09422298B2
出典データセットuspto-grants-2016_08
ORD IDord-23525637b4f04fb6a18f2c15dd65498f
出典メモuspto-grants-2016_08