돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1259832생성일: 2026년 10월 26일

Water → Rac-2-(tert-butoxycarbonylamino-methyl)-3-(7-fluoro-2-methoxy-quinolin-8-yl)-propionic acid ethyl ester

https://huagongshe.com/reaction/1259832

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Lithium HexamethyldisilazideHCID 2733832—
반응물Ethyl 3-{[(tert-butoxy)carbonyl]amino}propanoateHCID 15933116—
반응물8-(Bromomethyl)-7-fluoro-2-(methyloxy)quinolineHCID 66737650—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Rac-2-(tert-butoxycarbonylamino-methyl)-3-(7-fluoro-2-methoxy-quinolin-8-yl)-propionic acid ethyl esterHCID 6718170175%

반응 단계

To a solution of LiHMDS (1M, 20 mL), cooled to −78° C., was added dropwise a solution of 3-tert-butoxycarbonylamino-propionic acid ethyl ester (2.01 g, 9.26 mmol; prepared according to Tetrahedron Lett. (2003), 44(14), 2807) in THF (20 mL). The solution was stirred at the same temperature for 90 min. A solution of 8-bromomethyl-7-fluoro-2-methoxy-quinoline (2.5 g, 1 eq., prepared according to WO 2007/081597) in THF (10 mL) was quickly added and the reaction proceeded 2 h, keeping the internal temperature below −50° C. Water (100 mL) and EA (200 mL) were added. The two layers were separated and the aq. layer was extracted with EA. The combined org. layers were washed with brine, dried over Na2SO4, filtered and concentrated to dryness. The residue was purified by CC (Hept-EA 2-1) to afford the title intermediate as a pale yellow oil which solidified after standing at rt for one day (2.83 g, 75% yield). MS (ESI, m/z): 407.3 [M+H+].

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08466168B2
출처 데이터셋uspto-grants-2013_06
ORD IDord-5859d27fedf84df187a55bf7c8b9fad4
출처 메모uspto-grants-2013_06