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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1482234생성일: 2026년 10월 25일

Dimethylamine → Tert-butyl N2-(((9H-fluoren-9-YL)methoxy)carbonyl)-N5,N5-dimethyl-L-glutaminate

https://huagongshe.com/reaction/1482234

반응식

참여 물질

역할이름HCID투입량
반응물DimethylamineHCID 674—
반응물WaterHCID 962—
반응물DimethylformamideHCID 6228—
반응물Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphateHCID 151348—
반응물(S)-3-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-4-(tert-butoxy)-4-oxobutanoic acidHCID 7017910—
용매TetrahydrofuranHCID 8028—
생성물Tert-butyl N2-(((9H-fluoren-9-YL)methoxy)carbonyl)-N5,N5-dimethyl-L-glutaminateHCID 89668280—

반응 단계

(S)-3-((((9H-Fluoren-9-yl)methoxy)carbonyl)amino)-4-(tert-butoxy)-4-oxobutanoic acid (Compound SP444) (10.0 g, 23.5 mmol) was dissolved in dimethylformamide (70 ml), ((benzotriazol-1-yloxy)-tris(dimethylamino)phosphonium hexafluorophosphate (BOP) (12.5 g, 28.3 mmol) and dimethylamine (58 mmol) were added as a 2 mol/1 solution in tetrahydrofuran, and the mixture was stirred at room temperature for 30 minutes. Water was added to the reaction solution, followed by extraction with dichloromethane. The organic extract was dried over magnesium sulfate, and the solvent was evaporated under reduced pressure to afford tert-butyl (S)-2-((((9H-fluoren-9-yl)methoxy)carbonyl)amino)-5-(dimethylamino)-5-oxopentanoate (Compound SP447) (15.2 g) as a crude product.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US09409952B2
출처 데이터셋uspto-grants-2016_08
ORD IDord-4037fe8148704a29ae1f7fefb9d6590e
출처 메모uspto-grants-2016_08