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HRID 11565作成日:2026年10月24日

Citric Acid → {2-[(6-Cyano-pyridine-3-carbonyl)-amino]-phenyl}-carbamic acid t-butyl ester

https://huagongshe.com/ja/reaction/11565

反応式

関与物質

役割名称HCID仕込み量
反応物Citric AcidHCID 311—
反応物4-MethylmorpholineHCID 7972—
反応物Isobutyl chloroformateHCID 62365—
反応物N-(tert-Butoxycarbonyl)-1,2-phenylenediamineHCID 676311—
反応物6-Cyanopyridine-3-carboxylic acidHCID 2761108—
溶媒DimethylformamideHCID 6228—
生成物{2-[(6-Cyano-pyridine-3-carbonyl)-amino]-phenyl}-carbamic acid t-butyl esterHCID 6965566078.3%

反応条件

温度5 °C

反応手順

To a solution of 444 mg (3.0 mmol) 6-cyano-nicotinic acid and 354 mg (3.5 mmol) N-methylmorpholine in 7 ml DMF at −20° C. was added 450 mg (3.3 mmol) isobutyl chloroformate. The reaction mixture was warmed to 5° C., and 625 mg (3.0 mmol) mono-boc-ortho-phenylenediamine was added. The reaction mixture was warmed to rt overnight and then poured into 50 ml 5% aqueous citric acid. The aqueous phase was extracted with ethyl acetate, the combined organic phases were washed with bicarbonate and brine and dried over Na2SO4. The solvent was evaporated and the residue was subjected to silica gel chromatography (petrol ether/ethyl acetate 2:1) to yield 795 mg (2.35 mmol) {2-[(6-Cyano-pyridine-3-carbonyl)-amino]-phenyl}-carbamic acid t-butyl ester; mp.183–184° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07098247B2
出典データセットuspto-grants-2006_08
ORD IDord-0fe46712cd1942958efdafa5a636c66d
出典メモuspto-grants-2006_08