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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1611678생성일: 2026년 10월 27일

Triphenylphosphine → 8-(3-((2-Methylquinolin-8-yl)oxy)propoxy)quinolin-2-amine

https://huagongshe.com/reaction/1611678

반응식

참여 물질

역할이름HCID투입량
반응물TriphenylphosphineHCID 11776—
반응물2-Methyl-8-hydroxyquinolineHCID 13224—
반응물Dibenzyl azodicarboxylateHCID 5387121—
반응물3-((2-Aminoquinolin-8-yl)oxy)propan-1-olHCID 10353328—
용매TetrahydrofuranHCID 8028—
생성물8-(3-((2-Methylquinolin-8-yl)oxy)propoxy)quinolin-2-amineHCID 22254612—

반응 단계

A 20 mL scintillation vial with a septum cap was charged with PS-PPh3 resin (Aldrich Chemical Co., Inc, 60 mg, 2.4 equiv), 8-hydroxyquinaldine (1.5 equiv) and DBAD (28 mg, 1.6 equiv) and purged by passing a stream of N2 for 45 seconds. Anhydr. THF (3 mL) was added and the contents of the vial were shaken for 5 min. Then, a solution of 3-((2-aminoquinolin-8-yl)oxy)propan-1-ol (16.7 mg/mL; 1.0 mL, 0.077 mmol) in anhydr. THF (1 mL) was added and the resulting suspension was agitated at room temperature for 8 h. Then, PS-PPh3 resin (Aldrich Chemical Co., Inc, 60 mg, 2.4 equiv) and DBAD (28 mg, 1.6 equiv) were added and the mixture was agitated at room temperature for additional 6 h. The suspension was filtered, and the resin washed with THF (3×3.0 mL). The filtrate and washings were combined and evaporated in vacuo. The residue was then treated with 6.0 mL of 4 M HCl in dioxane at room temperature for 6 h. The resulting solution was evaporated in vacuo. The residue was dissolved in 1.5 mL of a 1:1 mixture of DMSO/MeOH and purified by preparative reverse-phase HPLC. 1H NMR (500 MHz, DMSO-d6) δ ppm 8.60 (d, 1H), 7.90 (d, 1H), 7.69 (t, 1H), 7.65 (d, 1H), 7.53 (d, 1H), 7.46 (d, 1H), 7.30 (t, 1H), 7.24 (m, 1H), 7.16 (m, 1H), 6.99 (d, 1H), 4.65 (br t, 2H), 4.48 (br t, 2H), 3.10 (s, 3H), 2.64 (m, 2H); MS (DCI/NH3) m/z 360 [M+H]+.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06989392B2
출처 데이터셋uspto-grants-2006_01
ORD IDord-5f4a86e55aaf472e824878b8e754c86a
출처 메모uspto-grants-2006_01