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HRID 511234作成日:2026年10月25日

Sodium Thiosulfate → 7-Amino-4-bromo-2-methylisoindolin-1-one

https://huagongshe.com/reaction/511234

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium ThiosulfateHCID 24477—
反応物N-bromobutanimideHCID 67184—
反応物7-Amino-2-methyl-2,3-dihydro-1H-isoindol-1-oneHCID 45088712—
溶媒DichloromethaneHCID 6344—
生成物7-Amino-4-bromo-2-methylisoindolin-1-oneHCID 5340845974%

反応手順

NBS (2.3 g, 12.96) was added to a cold (−8° C. to −10° C.) solution of 7-amino-2-methyl-2,3-dihydro-1H-isoindol-1-one (2 g, 12.4 mmol) in DCM (40 mL) and the mixture stirred at −8° C. to −10° C. for 1 h. A solution of 10% aq. sodium thiosulfate (30 mL) was then added to the reaction mixture and stirring was continued for another 20 minutes. The layers were separated and the aqueous layer was extracted with DCM (2×20 mL). The combined organic extracts were washed with water (3×40 mL) and brine (30 mL), and the organic layer was dried (Na2SO4) and concentrated in vacuo to yield 3.2 g of crude product. This material was triturated with ethyl acetate (10 mL) to give 2.2 g of pure 7-amino-4-bromo-2-methyl-2,3-dihydro-1H-isoindol-1-one (XXXIX, yield: 74%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09096624B2
出典データセットuspto-grants-2015_08
ORD IDord-dce05f2931924cd5b91ef7ab2c91aa50
出典メモuspto-grants-2015_08