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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 251729생성일: 2026년 10월 26일

(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine → tert-Butyl 6-[(2S,5R)-5-isopropyl-3,6-dimethoxy-2,5-dihydropyrazin-2-yl]hexanoate

https://huagongshe.com/reaction/251729

반응식

참여 물질

역할이름HCID투입량
반응물(R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazineHCID 736066—
반응물Tert-butyl 6-iodohexanoateHCID 12952475—
반응물ButyllithiumHCID 178418339—
용매TetrahydrofuranHCID 8028—
생성물tert-Butyl 6-[(2S,5R)-5-isopropyl-3,6-dimethoxy-2,5-dihydropyrazin-2-yl]hexanoateHCID 69227980—

반응 단계

To a stirred solution of (2R)-2-isopropyl-3,6-dimethoxy-2,5-dihydropyrazine (1.0 eq.) in THF at −78° C., was added dropwise over 10 min a solution of BuLi (1.6 N in hexane, 1.0 eq.) and stirring was continued at −78° C. for 45 min. A pre-cooled solution of tert-butyl 6-iodohexanoate (1.0 eq.) in THF was then added by cannula over 5 min and the reaction stirred overnight, slowly warming to RT. The reaction was then left to stir at RT for a further hour and was quenched by the addition of aqueous NH4Cl solution. The THF layer was decanted off and concentrated under reduced pressure, meanwhile and the aqueous mixture was extracted with EtOAc (3×). The EtOAc extracts were used to redissolve the oily THF residue and this solution was washed with brine, dried (Na2SO4) and concentrated under reduced pressure. The crude was used directly in the next step without further purification (I1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07863294B2
출처 데이터셋uspto-grants-2011_01
ORD IDord-2c34b75b684e4155920777c7fd1c69d2
출처 메모uspto-grants-2011_01