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HRID 2168998作成日:2026年10月26日

2-Chloroethyl vinyl ether → tert-butyl(3S,5R)-3-[({1-[2-(ethenyloxy)ethyl]-1H-benzimidazol-2-yl}carbonyl)(2-methylpropyl)amino]-5-(morpholin-4-ylcarbonyl)piperidine-1-carboxylate

https://huagongshe.com/reaction/2168998

反応式

関与物質

役割名称HCID仕込み量
反応物2-Chloroethyl vinyl etherHCID 8074—
反応物Cesium carbonateHCID 10796—
反応物tert-Butyl (3S,5R)-3-{(1H-benzimidazol-2-ylcarbonyl)(2-methylpropyl)amino)-5-(morpholin-4-ylcarbonyl)piperidine-1-carboxylateHCID 58355717—
触媒Potassium IodideHCID 4875—
溶媒WaterHCID 962—
溶媒DimethylacetamideHCID 31374—
生成物tert-butyl(3S,5R)-3-[({1-[2-(ethenyloxy)ethyl]-1H-benzimidazol-2-yl}carbonyl)(2-methylpropyl)amino]-5-(morpholin-4-ylcarbonyl)piperidine-1-carboxylateHCID 5835522892.3%

反応条件

温度60 °C

反応手順

To a solution of tert-butyl (3S,5R)-3-{(1H-benzimidazol-2-ylcarbonyl)(2-methylpropyl)amino}-5-(morpholin-4-ylcarbonyl)piperidine-1-carboxylate (308 mg), (2-chloroethoxy)ethene (192 mg) and potassium iodide (5 mg) in N,N-dimethylacetamide (5 ml) was added cesium carbonate (586 mg), and the mixture was stirred at 60° C. for 15 hr. The reaction mixture was cooled to room temperature, diluted with water, and extracted with ethyl acetate. The extract was washed with saturated brine, and dried over anhydrous sodium sulfate. The solvent was evaporated under reduced pressure. The residue was subjected to silica gel column chromatography, and a fraction eluted with ethyl acetate-hexane (6:4) was concentrated under reduced pressure to give the object product (323 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09045436B2
出典データセットuspto-grants-2015_06
ORD IDord-6c4d1e4c93cf47469fb269cf1ed77853
出典メモuspto-grants-2015_06