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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | (R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine | HCID 736066 | — |
| 반응물 | Tert-butyl 6-iodohexanoate | HCID 12952475 | — |
| 반응물 | Butyllithium | HCID 178418339 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | tert-Butyl 6-[(2S,5R)-5-isopropyl-3,6-dimethoxy-2,5-dihydropyrazin-2-yl]hexanoate | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07863294B2 |
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| 출처 데이터셋 | uspto-grants-2011_01 |
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| ORD ID | ord-2c34b75b684e4155920777c7fd1c69d2 |
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| 출처 메모 | uspto-grants-2011_01 |
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