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HRID 1507545作成日:2026年10月25日

Cesium carbonate → tert-butyl (3R)-3-[[5-(5-cyano-1,3-benzothiazol-2-yl)-6-methoxy-2-(morpholin-4-yl)pyrimidin-4-yl]amino]piperidine-1-carboxylate

https://huagongshe.com/reaction/1507545

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5-BenzothiazolecarbonitrileHCID 10702104—
反応物HCID 89554305HCID 89554305—
触媒Copper iodideHCID 83717—
触媒HCID 178418397HCID 178418397—
溶媒DimethylformamideHCID 6228—
生成物tert-butyl (3R)-3-[[5-(5-cyano-1,3-benzothiazol-2-yl)-6-methoxy-2-(morpholin-4-yl)pyrimidin-4-yl]amino]piperidine-1-carboxylateHCID 117686401—

反応手順

Following the same procedure as in step 3 of Example 121 using 1,3-benzothiazole-5-carbonitrile (56.1 mg, 0.35 mmol, 1.80 equiv), tert-butyl (3R)-3-[[5-iodo-6-methoxy-2-(morpholin-4-yl)pyrimidin-4-yl]amino]piperidine-1-carboxylate (100 mg, 0.19 mmol, 1.00 equiv), copper iodide (6.7 mg, 0.035 mmol, 0.18 equiv), cesium Carbonate (0.37 g, 6.00 equiv, 1.14 mmol) and Pd(PPh3)4 (40.4 mg, 0.035 mmol, 0.18 equiv) in DMF (6.0 mL). The crude product was purified by flash chromatography on silica gel, eluting with a mixture of 10-20% ethyl acetate in petroleum ether to give the title compound as a white solid. MS m/z [M+H]+ (ESI): 552.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09221809B2
出典データセットuspto-grants-2015_12
ORD IDord-33046ffc00a542da9c9c025694dd1f59
出典メモuspto-grants-2015_12