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HRID 1672994作成日:2026年10月27日

Potassium Carbonate → 2-chloro-4'-[2-(2,6-dichloro-phenyl)-5-isopropyl-2H-pyrazol-3-ylmethoxy]-biphenyl-4-carboxylic acid

https://huagongshe.com/reaction/1672994

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物SimtuzumabHCID 17750227—
反応物5-(4-bromophenoxymethyl)-1-(2,6-dichlorophenyl)-3-isopropyl-1H-pyrazoleHCID 59240102—
触媒HCID 178506421HCID 178506421—
溶媒Water 1,2-dimethoxyethaneHCID 18180031—
生成物2-chloro-4'-[2-(2,6-dichloro-phenyl)-5-isopropyl-2H-pyrazol-3-ylmethoxy]-biphenyl-4-carboxylic acidHCID 59240101—

反応条件

温度80 °C

反応手順

Into a 8 mL flask was added 200 mg (0.454 mmol) of 5-(4-bromophenoxymethyl)-1-(2,6-dichlorophenyl)-3-isopropyl-1H-pyrazole, 108 mg (0.54 mmol) of (4-carboxy-2-chlorophenyl)boronic acid, 186 mg of potassium carbonate (1.36 mmol) and 2 mL of 9:1 DME-water. The solution was sparged under argon and 6.5 mg (0.01 mmol) of palladium dppf was added. The reaction mixture was heated to 80° C. for 4 h. After cooling, the crude reaction was filtered through a pad of celite, concentrated in vacuo, and purified directly on a reverse phase HPLC-MS to afford 2-chloro-4′-[2-(2,6-dichlorophenyl)-5-isopropyl-2H-pyrazol-3-ylmethoxy]-biphenyl-4-carboxylic acid as an off white solid, yield (80.1 mg, 34%); 1H NMR (400 MHz, DMSO-d6): δ 13.37 (s, 1H), 8.04 (m, 1H), 7.96 (dd, J=8.1 (1.77) Hz, 1H), 7.73 (d J=8.1 Hz, 2H) 7.61 (m, 1H), 7.55 (d, J=7.83 Hz, 1H), 7.41 (d, J=8.84 Hz, 2H), 6.98 (d, J=9.09 Hz, 2H), 6.61 (s, 1H), 5.01 (s, 1H), 4.83 (s, 2H), 3.02 (m 1H), 2.52 (s, 1H), 1.31 (d J=6.82 Hz 6H), MS (ES): 515 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07998995B2
出典データセットuspto-grants-2011_08
ORD IDord-743fb86cd8c34fd9aead915bce12a777
出典メモuspto-grants-2011_08