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HRID 458214作成日:2026年10月25日

(2S)-2-(2,3,4-Trifluoroanilino)propanol → (3S)-3-Methyl-7,8-difluoro-2,3-dihydro-4H-1,4-benzoxazine

https://huagongshe.com/reaction/458214

反応式

関与物質

役割名称HCID仕込み量
反応物(2S)-2-(2,3,4-Trifluoroanilino)propanolHCID 11401466—
反応物Potassium tert-butoxideHCID 23665647—
溶媒DimethylformamideHCID 6228—
生成物(3S)-3-Methyl-7,8-difluoro-2,3-dihydro-4H-1,4-benzoxazineHCID 1104142479.8%

反応手順

To DMF (2 ml) was added potassium tertiary-butoxide (110 mg) under ice-cooling. Next, a solution of the compound (100 mg) obtained in Example 51 in DMF was dropped thereinto and the obtained mixture was stirred for 30 minutes. After treating in a conventional manner, the mixture was subjected to silica gel column chromatography to give 72 mg (79%) of the title compound. The optical purity determined by HPCL was >94% ee. Various spectral data was identical with those of a specimen synthesized separately.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07189847B2
出典データセットuspto-grants-2007_03
ORD IDord-e247380dea2547e99b893632047970af
出典メモuspto-grants-2007_03