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HRID 222766作成日:2026年10月26日

Iodoform → 1,1-Dimethylethyl 7-[(2-fluoro-4-Iodophenyl)oxy]-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate

https://huagongshe.com/reaction/222766

反応式

関与物質

役割名称HCID仕込み量
反応物IodoformHCID 6374—
反応物Tert-Butyl nitriteHCID 10906—
反応物1,1-Dimethylethyl 7-[(4-amino-2-fluorophenyl)oxy]-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylateHCID 58984568—
溶媒TetrahydrofuranHCID 8028—
生成物1,1-Dimethylethyl 7-[(2-fluoro-4-Iodophenyl)oxy]-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylateHCID 58984572—

反応手順

To a solution of 1,1-dimethylethyl 7-[(4-amino-2-fluorophenyl)oxy]-1,2,4,5-tetrahydro-3H-3-benzazepine-3-carboxylate (E274, Step 2) (0.5 g, 1.34 mmol) and iodoform (1 g, 2.69 mmol) in tetrahydrofuran (10 ml) was added dropwise tert-butyl nitrite (0.32 ml, 2.69 mmol). The reaction was then heated at reflux for 1 hour, cooled and concentrated in vacuo and resulting residue was purified by column chromatography eluting with a mixture of ethyl acetate:pentane (1:10) to afford the title compound. MS (ES+) m/e 384 [M-COOtBu]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08207331B2
出典データセットuspto-grants-2012_06
ORD IDord-58f1c6135a8b4fa39a18c13a6597f3f0
出典メモuspto-grants-2012_06