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HRID 7012作成日:2026年10月23日

Hydrochloric Acid → (spiro[cyclopentane-1,3'-[3H]indol]-2'(1'H)-one-5-yl)boronic acid

https://huagongshe.com/ja/reaction/7012

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物Triisopropyl borateHCID 21531—
反応物Sodium hydrideHCID 24758—
反応物5-Bromo-spiro [cyclopentane-1,3'-[3h]indol]-2'(1'h)-oneHCID 21986227—
反応物ButyllithiumHCID 178418339—
溶媒TetrahydrofuranHCID 8028—
生成物(spiro[cyclopentane-1,3'-[3H]indol]-2'(1'H)-one-5-yl)boronic acidHCID 2198624464%

反応条件

温度-78 °C

反応手順

To a solution of 5-bromo-spiro[cyclopentane-1,3′-[3H]indol]-2′(1′H)-one (13.1 g, 53 mmol) in anhydrous THF (300 cm3) under N2, was added sodium hydride (60% in mineral oil, 2.1 g, 53 mmol). After 30 minutes, the reaction mixture was cooled to −78° C. and butyl lithium (2.5 M in hexanes, 22 cm3, 53 mmol) was added slowly. After 30 minutes, tris-iso-propylborate (34 cm3, 146 mmol) was added, and the reaction mixture was slowly brought to room temperature, and stirred for 14 hours. The reaction mixture was poured into 1N HCl and extracted with EtOAc (×3). The organic layers were collected and washed with 1N HCl, water, dried (MgSO4) and evaporated to give the subtitled compound (7.8 g, 64%) as a tan solid which was used without further purification. 1H NMR (DMSO-d6) δ 10.3 (s, 1H), 7.9 (s, 1H), 7.7–7.6 (m, 2H), 6.8 (d, 1H, J=7.7 Hz), 3.4 (s, 1H), 2.0–1.7 (m, 8H); MS (FI-POS) m/z @231.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07084168B2
出典データセットuspto-grants-2006_08
ORD IDord-ed84227053dd4cc8ab8a2904657eb785
出典メモuspto-grants-2006_08