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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17100생성일: 2026년 10월 26일

Trifluoroacetic acid → 2-((6-Bromopyridin-2-yl)methyl)isoindoline-1,3-dione

https://huagongshe.com/reaction/17100

반응식

참여 물질

역할이름HCID투입량
반응물Trifluoroacetic acidHCID 6422—
반응물PhthalimideHCID 6809—
반응물TriphenylphosphineHCID 11776—
반응물1,1'-(Azodicarbonyl)dipiperidineHCID 73042—
반응물(6-Bromopyridin-2-yl)methanolHCID 3517811—
용매MethanolHCID 887—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물2-((6-Bromopyridin-2-yl)methyl)isoindoline-1,3-dioneHCID 22176446—

반응 단계

A mixture of commercially available (6-bromopyridin-2-yl)methanol (20.0 g, 0.106 mol), phthalimide (20.4 g, 0.138 mol), and triphenylphosphine (36.2 g, 0.138 mol), and 1,1′-(azodicarbonyl)-dipiperidine (34.8 g, 0.138 mol) in anhydrous tetrahydrofuran (1 L) was stirred at room temperature overnight. The precipitate was collected by vacuum filtration and washed with tetrahydrofuran. The filtrate was concentrated under reduced pressure, and the solid residue was triturated with methanol with sonication. A214.1 was collected by vacuum filtration and was dried well to give 24.1 g as a white solid. The filtrate still contained significant product which could be isolated as a second crop with methanol trituration. The compound had an HPLC retention time=2.32 min. (Column: Chromolith SpeedROD 4.6×50 mm—4 min.; Solvent A=10% MeOH, 90% H2O, and 0.1% TFA; Solvent B=90% MeOH, 10% H2O, and 0.1% TFA) and a LC/MS M+1=317.15 and 319.15.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737279B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-b3467d2092bb4e8c87455c945af69572
출처 메모uspto-grants-2010_06