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HRID 527955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/527955

反応式

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-oneHCID 2763681—
反応物(S)-Glycidoxy-t-butyldimethylsilaneHCID 10954307—
溶媒AcetonitrileHCID 6342—
生成物6-[(S)-3-(tert-butyl-dimethyl-silanyloxy)-2-hydroxy-propylamino]-4H-benzo[1,4]oxazin-3-oneHCID 6673769566.1%

反応条件

温度50 °C

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US09346804B2
出典データセットuspto-grants-2016_05
ORD IDord-f62c9553bde44f8aaa78ba59e9b288fd
出典メモuspto-grants-2016_05