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HRID 1725928作成日:2026年10月27日

Toluene → 5,6-Disubstituted anthranilic acid sulfonamide, 9e

https://huagongshe.com/reaction/1725928

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Butylboronic AcidHCID 20479—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Benzyl 3-bromo-6-{[(4-fluorophenyl)sulfonyl]amino}-2-methylbenzoateHCID 68864112—
触媒HCID 178479803HCID 178479803—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
生成物5,6-Disubstituted anthranilic acid sulfonamide, 9eHCID 23647765—

反応条件

温度100 °C

反応手順

A mixture of Example 225A (123 mg, 0.26 mmol), potassium phosphate (192 mg, 0.9 mmol), butylboronic acid (34 mg, 0.33 mmol), bis(tricyclohexylphosphino)palladium dichloride (19 mg, 0.03 mmol), toluene (4 mL), and water (0.2 mL) was purged with argon and shaken at 100° C. for 36 hours in a sealed container. The mixture was diluted with ethyl acetate (10 mL), washed with water (2×10 mL) and brine, dried (Na2SO4), filtered, concentrated and passed through a silica gel cartridge (20 g) with 15% ethyl acetate/hexanes. The isolated solid was substituted for Example 108C in Example 108D and purified by preparative HPLC on a Waters Symmetry C8 column (25 mm×100 mm, 7 μm particle size) using a gradient of 10% to 100% acetonitrile/0.1% aqueous TFA over 8 minutes (10 minute run time) at a flow rate of 40 mL/min to provide the desired-product. MS (ESI(+)) m/e 383 (M+NH4)+; (ESI(−)) m/e 364 (M−H)−; 1H NMR (300 MHz, DMSO-d6) δ 13.09 (br s, 1H), 9.74 (br s, 1H), 7.78 (m, 2H), 7.39 (m, 2H), 7.08 (d, 1H), 6.71 (d, 1H), 2.55 (q, 2H), 2.18 (s, 3H), 1.44 (m, 2H), 1.32 (m, 2H), 0.91 (t, 3H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07491718B2
出典データセットuspto-grants-2009_02
ORD IDord-ae1c384e886e4e6883cc58838382736c
出典メモuspto-grants-2009_02