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HRID 81283作成日:2026年10月26日

Cesium carbonate → HCID 178461220、化合物

https://huagongshe.com/reaction/81283

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium carbonateHCID 10796—
反応物CyclobutylcarbinolHCID 78130—
反応物Binap, (A+-)-HCID 634876—
反応物HCID 178461219HCID 178461219—
触媒Bis(dibenzylideneacetone)palladiumHCID 9811564—
溶媒Dimethyl SulfoxideHCID 679—
生成物HCID 178461220HCID 178461220—

反応条件

温度100 °C

反応手順

To a solution of 4,6-dichloro-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine (Example 2.1, Step 2; 400 mg, 0.87 mmol) in DMSO (5 mL) was added cyclobutylmethanol (337 mg, 3.92 mmol), Cs2CO3 (848 mg, 2.61 mmol) and BINAP (108 mg, 0.17 mmol). The reaction mixture was deoxygenated by purging with nitrogen for 10 minutes and then Pd2dba3 (159 mg, 0.17 mmol) was added. The reaction was again deoxygenated for 5 minutes by purging with nitrogen. The reaction flask was sealed, and the mixture was heated at 100° C. for 16 h. The reaction mixture was then cooled, diluted with water (30 ml) and EtOAc (60 mL), and the organic layer was separated. The organic layer was washed with water (2×10 mL), followed by saturated brine (2×30 mL). The organic layer was dried over anhydrous Na2SO4, filtered, and concentrated. The residue was purified on a silica gel column (30% EtOAc/petroleum ether) to yield 6-chloro-4-(cyclobutylmethoxy)-3-[(trans-4-methylcyclohexyl)methyl]-2-[(3R)-3-phenylmorpholin-4-yl]-3H-imidazo[4,5-c]pyridine. MS ES/APCl calc'd. for C29H37ClN4O2 [M+H]+ 509. found 509.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08846657B2
出典データセットuspto-grants-2014_09
ORD IDord-4080d3e218c94089919b724dd34a35eb
出典メモuspto-grants-2014_09