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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 651054생성일: 2026년 10월 27일

Oxycinchophen → Talnetant

https://huagongshe.com/reaction/651054

반응식

참여 물질

역할이름HCID투입량
반응물OxycinchophenHCID 10239—
반응물DicyclohexylcarbodiimideHCID 10868—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물(1S)-1-phenylpropan-1-amineHCID 6993773—
용매DichloromethaneHCID 6344—
용매TetrahydrofuranHCID 8028—
생성물TalnetantHCID 531142448.7%

반응 단계

2.49 g (9.4 mmol) of 3-hydroxy-2-phenylquinoline-4-carboxylic acid (CAS [485-89-2]) were suspended in 150 ml of a 7/3 mixture of THF/CH3CH; 1.40 g (10.3 mmol) of 1-hydroxybenzotriazole (HOBT) and 1.27 g (9.4 mmol) of (S)-α-ethylbenzylamine dissolved in 20 ml of CH2Cl2 were added and the reaction mixture was stirred at room temperature for 30 minutes. 2.13 g (10.3 mmol) of dicyclohexylcarbodiimide (DCC) dissolved in 20 ml of CH2Cl2 were added dropwise. The reaction was left at room temperature overnight, quenched with 20 ml of H2O, evaporated in-vacuo to dryness and dissolved in EtOAc. The precipitated dicyclohexylurea was filtered off and the organic layer was washed with H2O, 20% citric acid, sat. sol. NaHCO3, sat. sol. NaCl. The organic layer was separated, dried over Na2SO4 and evaporated in-vacuo to dryness; the residue was purified by gradient column chromatography on 60-240 mesh silica gel using a mixture of hexane/EtOAc 9:1 as starting eluent and a mixture of hexane/EtOAc 7:3 as final eluent. The crude product was recrystallized from i-PrOH to yield 1.75 g of the title compound as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06277862B1
출처 데이터셋uspto-grants-2001_08
ORD IDord-0f001969ad0c447b9c251351b1f18450
출처 메모uspto-grants-2001_08