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HRID 1802569作成日:2026年10月27日

1,2-Dichloroethane → Benzyl 9-(5-{[(2-aminophenyl)amino]carbonyl}pyridin-2-yl)-3,9-diazaspiro[5.5]-undecane-3-carboxylate

https://huagongshe.com/reaction/1802569

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DichloroethaneHCID 11—
反応物O-PhenylenediamineHCID 7243—
反応物TriethylamineHCID 8471—
反応物Benzyl chloroformateHCID 10387—
反応物1-HydroxybenzotriazoleHCID 75771—
反応物Lithium hydroxide, monohydrateHCID 168937—
反応物Tert-butyl 9-[5-(methoxycarbonyl)pyridin-2-yl]-3,9-diazaspiro[5.5]undecane-3-carboxylateHCID 57717452—
溶媒DichloromethaneHCID 6344—
溶媒Trifluoroacetic acidHCID 6422—
溶媒Methanol tetrahydrofuran waterHCID 21892291—
生成物Benzyl 9-(5-{[(2-aminophenyl)amino]carbonyl}pyridin-2-yl)-3,9-diazaspiro[5.5]-undecane-3-carboxylateHCID 57717481—

反応手順

A solution of tert-butyl 9-[5-(methoxycarbonyl)pyridin-2-yl]-3,9-diazaspiro[5.5]undecane-3-carboxylate (100 mg, 0.257 mmol) in 1 mL of CH2Cl2 and 1 mL of TFA was stirred for 1 h and concentrated. The oil was redissolved in 2 mL of CH2Cl2 and treated with NEt3 (0.15 mL, 1.08 mmol) and CbzCl (0.060 mL, 0.42 mmol), then stirred for 8 h. The mixture was partitioned between EtOAc and sat'd NaHCO3, dried (Na2SO4), filtered and concentrated. The residue was stirred in 3 mL of 1:1:1 MeOH/THF/water with LiOH.H2O (30 mg, 0.71 mmol) for 10 h, concentrated to dryness, dissolved in 2 mL of DMF, treated with EDC (150 mg, 0.79 mmol), HOBt (100 mg, 0.74 mmol), and phenylenediamine (100 mg, 0.93 mmol). The mixture was stirred for 18 h, concentrated, and triturated with methanol giving the title compound; MS (ESI+): cal'd [M+1]+ 500.3, obs'd 500.3.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08349825B2
出典データセットuspto-grants-2013_01
ORD IDord-2d9448d38eed4dd5b9d6b048baa9b3cf
出典メモuspto-grants-2013_01