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HRID 1916314作成日:2026年10月27日
6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-one → 6-[(S)-3-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-propylamino]-4H-benzo[1,4]oxazin-3-one
https://huagongshe.com/reaction/1916314
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | 6-amino-3,4-dihydro-2H-1,4-benzoxazin-3-one | HCID 2763681 | — |
| 反応物 | (S)-Glycidoxy-t-butyldimethylsilane | HCID 10954307 | — |
| 溶媒 | Acetonitrile | HCID 6342 | — |
| 生成物 | 6-[(S)-3-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-propylamino]-4H-benzo[1,4]oxazin-3-one | HCID 66737695 | 66.1% |
反応手順
LiClO4 (7.20 g, 3 eq.) was added to a solution of tert-butyl-dimethyl-((S)-1-oxiranylmethoxy)-silane (commercial; 4.25 g, 22.6 mmol) in MeCN (70 mL). 6-amino-4H-benzo[1,4]oxazin-3-one (commercial; 3.70 g, 1 eq.) was then added and the mixture was stirred at 50° C. for 6 h. The solvent was removed under reduced pressure and the residue was purified by CC (DCM/MeOH/NH4OH 1000/25/2) to afford the title intermediate as a pale brown foam (5.25 g, 66% yield).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08618092B2 |
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| 出典データセット | uspto-grants-2013_12 |
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| ORD ID | ord-371d34d337974cf39f31cc8347bd3773 |
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| 出典メモ | uspto-grants-2013_12 |
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