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HRID 571445作成日:2026年10月27日

tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-1-carboxylate → 1-BOC-Indazole-5-boronic acid

https://huagongshe.com/reaction/571445

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl 5-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-indazole-1-carboxylateHCID 18525862—
溶媒Propan-2-one--water (1/1)HCID 18366337—
生成物1-BOC-Indazole-5-boronic acidHCID 6742505268%

反応手順

To N-Boc-indazole-5-boronic acid pinacol ester (S46) (390 mg, 1.13 mmol, 1.00 equiv) in acetone/H2O (5.0 mL/5.0 mL) at 23° C. was added NH4OAc (436 mg, 5.65 mmol, 5.00 equiv) and NaIO4 (1.21 g, 5.65 mmol, 5.00 equiv). After stiffing for 48 hr at 23° C., the reaction mixture was concentrated in vacuo to remove acetone. To the residual solution was added EtOAc (5 mL) and the phases were separated. The aqueous phase was extracted with EtOAc (2×5 mL). The combined organic phases are washed with brine (10 mL) and dried (Na2SO4). The filtrate was concentrated in vacuo and the residue was triturated with Et2O to afford 200 mg of the title compound as a colorless solid (68% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09024093B2
出典データセットuspto-grants-2015_05
ORD IDord-90458706fc9e4692b04136d2a565b03b
出典メモuspto-grants-2015_05