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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 870494생성일: 2026년 10월 27일

Oxalic Acid → (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine ethanedioate

https://huagongshe.com/reaction/870494

반응식

참여 물질

역할이름HCID투입량
반응물Oxalic AcidHCID 971—
반응물(2S)-5-[(benzyloxy)amino]-2-cyanopiperidineHCID 117599345—
용매AcetoneHCID 180—
용매Ethyl AcetateHCID 8857—
생성물(2S)-5-[(benzyloxy)amino]-2-cyanopiperidine ethanedioateHCID 131732538—

반응 단계

The compound of Formula (IX) was reacted with sulphuric acid and sodium triacetoxy borohydride, in presence of suitable solvent such as ethyl acetate and at temperature below −5° C., to provide (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine (X). The compound of Formula (X) was purified by forming oxalate salt. The compound of Formula (X) was reacted with oxalic acid in a mixture of ethylacetate and acetone to provide (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine ethanedioate (1:1) (XI), which was further treated with sodium hydrogen carbonate to obtain purified (2S)-5-[(benzyloxy)amino]-2-cyanopiperidine (XII). The racemic compound (XI) was treated with methanol to obtain pure (2S,5R)-5-[(benzyloxy)amino]-2-cyanopiperidine ethanedioate.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08969567B2
출처 데이터셋uspto-grants-2015_03
ORD IDord-a693cc2549d2401c8dbd9b3957b1cbfd
출처 메모uspto-grants-2015_03