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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 20039생성일: 2026년 10월 23일

Dichloromethane → 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

https://huagongshe.com/ko/reaction/20039

반응식

참여 물질

역할이름HCID투입량
반응물DichloromethaneHCID 6344—
반응물Trimethyl orthoformateHCID 9005—
반응물Sodium triacetoxyborohydrideHCID 5049666—
반응물(S)-2,2-dimethyl-6-neopentyl-1,2,3,4-tetrahydroquinolin-4-amineHCID 67305468—
반응물tert-butyl (2S,3S)-3-(tert-butyldimethylsilyloxy)-1-(3-fluorophenyl)-4-oxobutan-2-ylcarbamateHCID 86614118—
생성물Tert-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—

반응 단계

To a solution of tert-butyl (2S,3S)-3-(tert-butyldimethylsilyloxy)-1-(3-fluorophenyl)-4-oxobutan-2-ylcarbamate (0.148 g, 0.360 mmol) and (S)-2,2-dimethyl-6-neopentyl-1,2,3,4-tetrahydroquinolin-4-amine (0.0886 g, 0.360 mmol) in DCM (7.19 ml, 0.360 mmol) was added trimethoxymethane (0.394 ml, 3.60 mmol). The resulting solution was stirred for 1 hour at which time, sodium triacetoxyborohydride (0.229 g, 1.08 mmol) was added. The solution was then stirred for 30 minutes, quenched with saturated Rochelle's salt and stirred for an additional 20 minutes. The mixture was transferred to a sep. funnel containing DCM and H2O. The aqueous layer was washed 4× with DCM. The organic layers were combined, washed 1× with brine, dried with MgSO4, filtered and concentrated to afford the title compound. MS m/z: 642 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07745484B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-0feb4bd794af4aba8348f04397537e43
출처 메모uspto-grants-2010_06