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HRID 251729作成日:2026年10月27日
(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
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
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| 反応物 | (R)-2,5-Dihydro-3,6-dimethoxy-2-isopropylpyrazine | HCID 736066 | — |
| 反応物 | Tert-butyl 6-iodohexanoate | HCID 12952475 | — |
| 反応物 | Butyllithium | HCID 178418339 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | tert-Butyl 6-[(2S,5R)-5-isopropyl-3,6-dimethoxy-2,5-dihydropyrazin-2-yl]hexanoate | HCID 69227980 | — |
反応手順
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).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07863294B2 |
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| 出典データセット | uspto-grants-2011_01 |
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| ORD ID | ord-2c34b75b684e4155920777c7fd1c69d2 |
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| 出典メモ | uspto-grants-2011_01 |
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