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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20040생성일: 2026년 10월 23일

Dichloromethane → Tert-butyl (2S,3R)-4-((S)-2,2-dimethyl-6-neopentyl-1,2,3,4-tetrahydroquinolin-4-ylamino)-1-(3-fluorophenyl)-3-hydroxybutan-2-ylcarbamate

https://huagongshe.com/ko/reaction/20040

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Ethyl AcetateHCID 8857—
반응물Tetrabutylammonium FluorideHCID 2724141—
반응물Tert-butyl (2S,3R)-3-(tert-butyldimethylsilyloxy)-4-((S)-2,2-dimethyl-6-neopentyl-1,2,3,4-tetrahydroquinolin-4-ylamino)-1-(3-fluorophenyl)butan-2-ylcarbamateHCID 86614130—
용매WaterHCID 962—
생성물Tert-butyl (2S,3R)-4-((S)-2,2-dimethyl-6-neopentyl-1,2,3,4-tetrahydroquinolin-4-ylamino)-1-(3-fluorophenyl)-3-hydroxybutan-2-ylcarbamateHCID 86614131—

반응 단계

To a solution of tert-butyl (2S,3R)-3-(tert-butyldimethylsilyloxy)-4-((S)-2,2-dimethyl-6-neopentyl-1,2,3,4-tetrahydroquinolin-4-ylamino)-1-(3-fluorophenyl)butan-2-ylcarbamate (0.231 g, 0.360 mmol) in DCM (1.20 ml, 0.360 mmol) was added tetrabutylammonium fluoride (1.44 ml, 1.44 mmol). The resulting solution was stirred overnight. The mixture was transferred to a sep. funnel containing EtOAc and H2O. The aqueous layer was washed 4× with EtOAc. The proganic layers were combined, dried over MgSO4, filtered and concentrated. The crude mixture was purified by the MPLC. MS m/z: 528 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745484B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-3dc081c328df412bb63db52a60eba9d2
출처 메모uspto-grants-2010_06