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HRID 2105612作成日:2026年10月25日

Benzo(B)Thiophene-2-Boronic Acid → (4-Benzo[b]thiophen-2-yl-pyridin-2-yl)-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-amine

https://huagongshe.com/reaction/2105612

反応式

関与物質

役割名称HCID仕込み量
反応物Benzo(B)Thiophene-2-Boronic AcidHCID 2359—
反応物(2,3-Dihydro-benzo[1,4]dioxin-6-yl)-(4-iodo-pyridin-2-yl)-amineHCID 57808271—
触媒Tetrakis(triphenylphosphine)palladiumHCID 11979704—
溶媒1,2-DimethoxyethaneHCID 8071—
生成物(4-Benzo[b]thiophen-2-yl-pyridin-2-yl)-(2,3-dihydro-benzo[1,4]dioxin-6-yl)-amineHCID 57808231—

反応条件

温度150 °C

反応手順

Following the same procedure described for Example 401(c), the mixture of (2,3-dihydro-benzo[1,4]dioxin-6-yl)-(4-iodo-pyridin-2-yl)-amine (Example 401(b), 75 mg, 0.2 mmol), tetrakis (triphenylphosphine) palladium (0) (Aldrich Chemical Company) (12 mg, 0.011 mmol), benzothiophene-2-boronic acid (Frontier Scientific, Inc.) (45 mg, 0.25 mmol) and 1,2-dimethoxyethane (2 mL) gave, after heated in the Microwave Smith Synthesizer at 150° C. for 10 min and purification on a Biotage 40S column (4:1 hexane:EtOAc), the title compound as a light-yellow solid. MS (ESI, pos. ion) m/z: 361 (M+1). Mp: 154.0-154.1° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07579347B2
出典データセットuspto-grants-2009_08
ORD IDord-e898ca49f24144a08b1aec25573011b2
出典メモuspto-grants-2009_08