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HRID 244739作成日:2026年10月24日

Acetonitrile → HCID 58356419、化合物

https://huagongshe.com/ja/reaction/244739

反応式

関与物質

役割名称HCID仕込み量
反応物AcetonitrileHCID 6342—
反応物Pentapotassium TriphosphateHCID 61695—
反応物Benzofuran, 5-bromo-HCID 90015—
反応物HCID 58255833HCID 58255833—
触媒HCID 178420574HCID 178420574—
溶媒WaterHCID 962—
溶媒1,4-DioxaneHCID 31275—
生成物HCID 58356419HCID 5835641910.7%

反応手順

2-methyl-N-[2-(tetrahydro-2H-pyran-2-yl)-6-(4,4,6,6-tetramethyl-1,3,2-dioxaborinan-2-yl)-2H-indazol-4-yl]-1,3-thiazole-4-carboxamide (53 mg, 0.11 mmol) was dissolved in 1,4-Dioxane (0.4 mL) and added to 5-bromo-1-benzofuran (20 mg, 0.1 mmol, available from ABCR) in a microwave vessel. 1,4-Dioxane (0.4 ml) was added followed by chloro[2′-(dimethylamino)-2-biphenylyl]palladium-(1R,4S)-bicyclo[2.2.1]hept-2-yl[(1S,4R)-bicyclo[2.2.1]hept-2-yl]phosphane (1:1) (Solvias catalyst, 2 mg, 0.004 mmol, (heaped microspatula) available from ABCR) and a solution of potassium triphosphate (0.2 g, 0.1 mmol) in water (0.2 ml). The vessel was sealed and heated in CEM Discover using initial 150 W to 110° C. for 20 min. After cooling the solution was loaded onto a C18 SPE cartridge (pre-conditioned with MeCN/0.1% TFA) and flushed through with a further 3 ml MeCN/0.1% TFA. Solvent was removed by blowdown under a stream of nitrogen. The residue was dissolved in MeOH (0.51) and loaded onto a SCX-2 SPE cartridge (1 g) pre-conditioned with MeOH. The material was left on the column for 1 hr then eluted with 2M ammonia/MeOH and evaporated to dryness. The sample was purified by Mass Directed AutoPrep (Method C) to afford the title compound (4 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658635B2
出典データセットuspto-grants-2014_02
ORD IDord-32355e155b92499f906cc13497886f0f
出典メモuspto-grants-2014_02