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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 476230생성일: 2026년 10월 26일

Diisopropylethylamine → 2-(4-Fluorophenyl)propionic acid

https://huagongshe.com/reaction/476230

반응식

참여 물질

역할이름HCID투입량
반응물DiisopropylethylamineHCID 81531—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물propyl [(7R)-7-(methylamino)-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl]acetateHCID 86655417—
용매DimethylformamideHCID 6228—
생성물2-(4-Fluorophenyl)propionic acidHCID 2723915—

반응 단계

(33 mg) and HATU (76 mg) were dissolved in DMF (1.3 mL). DIPEA (87 μL, 0.315 mmol) was added and the mixture was stirred for 1 min before the addition of propyl [(7R)-7-(methylamino)-6,7,8,9-tetrahydropyrido[1,2-a]indol-10-yl]acetate (50 mg) in 1 mL DMF. The reaction mixture was stirred for 2 h. The solvent was removed under vacuum and the residue was purified on silica gel (ethyl acetate/hexanes). The resulting diastereoisomers were separated on a Chiralpak AD column (20% iPrOH/Hexanes, 0.25% HCOOH). The propyl esters were hydrolysed to their corresponding acids using a procedure analogous to the one described in Step 2. MS (+ESI) m/z: 409.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08637671B2
출처 데이터셋uspto-grants-2014_01
ORD IDord-2e430c3310ff4cfc95166c1f0f1e9cc4
출처 메모uspto-grants-2014_01