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HRID 246750作成日:2026年10月24日

Dibutylchloro(propyl)stannane → 5-(difluoromethoxy)-3-(tributylstannyl)-1H-indazole

https://huagongshe.com/ja/reaction/246750

反応式

関与物質

役割名称HCID仕込み量
反応物Dibutylchloro(propyl)stannaneHCID 59914830—
反応物3-(5-(difluoromethoxy)-3-iodo-1H-indazol-1-yl)-N,N-dimethylpropan-1-amineHCID 71279816—
反応物HCID 178418918HCID 178418918—
溶媒TetrahydrofuranHCID 8028—
生成物5-(difluoromethoxy)-3-(tributylstannyl)-1H-indazoleHCID 178448231—

反応手順

To a solution of 3-(5-(difluoromethoxy)-3-iodo-1H-indazol-1-yl)-N,N-dimethylpropan-1-amine (1.2 g, 2.78 mmol) in dry THF (25 mL) was added isopropylmagnesium chloride (1.5 mL, 2M in THF, 3 mmol) drop-wise at −16° C. under nitrogen atmosphere. The reaction was stirred for 30 minutes, then dibutylchloro (propyl)stannane (3.3 mL, 3.6 mmol) was added dropwise at −16° C. under nitrogen, then the reaction mixture was slowly warmed to room temperature and stirred for 2 hours. The reaction mixture was quenched with a solution of saturated NH4Cl (40 mL) and product extracted with EtOAc (3×30 mL), organics combined dried with sodium sulfate, filtered and concentrated. Crude oil used into the next step without further purification (1.1 g, crude).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08658646B2
出典データセットuspto-grants-2014_02
ORD IDord-564934e42e8c41d48052eebbcfd37fb0
出典メモuspto-grants-2014_02