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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2360564생성일: 2026년 10월 25일

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/2360564

반응식

참여 물질

역할이름HCID투입량
반응물1,2-DichloroethaneHCID 11—
반응물O-PhenylenediamineHCID 7243—
반응물TriethylamineHCID 8471—
반응물Benzyl chloroformateHCID 10387—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물Lithium hydroxide, monohydrateHCID 168937—
반응물Tert-butyl 9-[5-(methoxycarbonyl)pyridin-2-yl]-3,9-diazaspiro[5.5]undecane-3-carboxylateHCID 57717452—
용매DichloromethaneHCID 6344—
용매Trifluoroacetic acidHCID 6422—
용매Methanol tetrahydrofuran waterHCID 21892291—
생성물Benzyl 9-(5-{[(2-aminophenyl)amino]carbonyl}pyridin-2-yl)-3,9-diazaspiro[5.5]-undecane-3-carboxylateHCID 57717481—

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08686020B2
출처 데이터셋uspto-grants-2014_04
ORD IDord-cf65e9b902bc483cb9e3c679c6657575
출처 메모uspto-grants-2014_04