돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1782013생성일: 2026년 10월 23일

Hydrochloric Acid → tert-butyl (3S,4R)-4-amino-3-fluoropiperidine-1-carboxylate

https://huagongshe.com/ko/reaction/1782013

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물cis-4-Benzylamino-1-tert-butoxycarbonyl-3-fluoropiperidineHCID 11312869—
촉매PalladiumHCID 23938—
용매EthanolHCID 702—
생성물tert-butyl (3S,4R)-4-amino-3-fluoropiperidine-1-carboxylateHCID 1173610453%

반응 단계

To a solution of the enantiomeric mixture of cis-4-benzylamino-1-tert-butoxycarbonyl-3-fluoropiperidine (prepared according to the procedures of J. Med. Chem. 1999, 42, 2087-2104, 1.0 g, 3.2 mmole) in EtOH (40 mL) was added 3 N HCl (2.5 L) and 10% Pd/C (50 mg). The reaction was shaken under H2 (40 psi) on a Parr apparatus for 14 h, then was filtered through Celite®. The filtrate was concentrated under reduced pressure, and the residue was purified by flash chromatography on silica gel (10% MeOH/CHCl3) to afford the title compound (370 mg, 53%) as a white solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07498326B2
출처 데이터셋uspto-grants-2009_03
ORD IDord-22eb2861c23d43d680bdd14f2f88c5d2
출처 메모uspto-grants-2009_03