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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1725928생성일: 2026년 10월 26일

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

https://huagongshe.com/reaction/1725928

반응식

참여 물질

역할이름HCID투입량
반응물TolueneHCID 1140—
반응물Butylboronic AcidHCID 20479—
반응물Potassium Phosphate, TribasicHCID 62657—
반응물Benzyl 3-bromo-6-{[(4-fluorophenyl)sulfonyl]amino}-2-methylbenzoateHCID 68864112—
촉매HCID 178479803HCID 178479803—
용매WaterHCID 962—
용매Ethyl AcetateHCID 8857—
생성물5,6-Disubstituted anthranilic acid sulfonamide, 9eHCID 23647765—

반응 조건

온도100 °C

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07491718B2
출처 데이터셋uspto-grants-2009_02
ORD IDord-ae1c384e886e4e6883cc58838382736c
출처 메모uspto-grants-2009_02