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HRID 1525507作成日:2026年10月26日

Dimethylformamide → tert-Butyl 4-bromo-1H-pyrrolo[2,3-b]pyridine-1-carboxylate

https://huagongshe.com/reaction/1525507

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Trifluoromethanesulfonic anhydrideHCID 67749—
反応物4-Bromo-1H-pyrrolo[2,3-b]pyridineHCID 22273643—
反応物HCID 178526243HCID 178526243—
触媒Tetrabutylammonium BromideHCID 74236—
生成物tert-Butyl 4-bromo-1H-pyrrolo[2,3-b]pyridine-1-carboxylateHCID 5829832034.3%

反応条件

温度0 °C

反応手順

4-Bromo-1H-pyrrolo[2,3-b]pyridine. A solution of trifluoromethyl sulfonic anhydride (9.3 g, 33 mmol) was added dropwise to a mixture of 1H-pyrrolo[2,3-b]pyridine 7-oxide (3 g, 22 mmol) and tetrabutyl ammonium bromide (10.8 g, 33 mmol) in N,N-dimethylformamide (30 mL) at 0° C. The resulting mixture was stirred at 0° C. for 4 h and at room temperature overnight. The reaction was quenched with water and neutralized with 1N sodium hydroxide to pH=7. The resulting mixture was extracted twice with a mixture of methylene chloride and i-propanol (30 mL, Vm:Vp=4:1). The organic layer was combined, dried over anhydrous sodium sulfate, concentrated and purified by a reverse-phase preparatory HPLC (0-30%: acetonitrile+0.1% TFA in water+0.1% TFA, over 15 min.) to give the title compound (1.5 g, 34.3% yield). MS (ESI) m/z 196.8 [M+1]+, 198.8 [M+3]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09079900B2
出典データセットuspto-grants-2015_07
ORD IDord-7b2c7220db94449da43c987c9911f845
出典メモuspto-grants-2015_07