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HRID 221760作成日:2026年10月27日

((S)-5-{5-[(5-Cyano-pyridine-2-carbonyl)-amino]-2-fluoro-phenyl}-5-difluoromethyl-2,5,6,7-tetrahydro-[1,4]oxazepin-3-yl)-carbamic acid tert-butyl ester → Ethanol heptane

https://huagongshe.com/reaction/221760

反応式

関与物質

役割名称HCID仕込み量
反応物((S)-5-{5-[(5-Cyano-pyridine-2-carbonyl)-amino]-2-fluoro-phenyl}-5-difluoromethyl-2,5,6,7-tetrahydro-[1,4]oxazepin-3-yl)-carbamic acid tert-butyl esterHCID 66666436—
溶媒DichloromethaneHCID 6344—
溶媒Trifluoroacetic acidHCID 6422—
生成物Ethanol heptaneHCID 22502148244.9%

反応手順

((S)-5-{5-[(5-Cyano-pyridine-2-carbonyl)-amino]-2-fluoro-phenyl}-5-difluoromethyl-2,5,6,7-tetrahydro-[1,4]oxazepin-3-yl)-carbamic acid tert-butyl ester (67.7 mg, 0.134 mmol) was dissolved in 0.75 mL dichloromethane and 0.25 mL trifluoroacetic acid. The solution was stirred at for 45 minutes and then evaporated at room temperature. The residue was dissolved in EtOAc and extracted with saturated aqueous NaHCO3 solution. The layers were washed with brine and EtOAc. The combined organic layers were dried over Na2SO4 and evaporated. The crude product was dissolved in THF, 0.2 mL HCl solution 1 mol/L in diethyl ether was added and the mixture was evaporated. The residue was crystallized from ethanol and TBME to give 48 mg of the title compound as white crystals.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207164B2
出典データセットuspto-grants-2012_06
ORD IDord-586a144163db44618412439093ae75c4
出典メモuspto-grants-2012_06