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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 419207생성일: 2026년 10월 24일

2-Fluoro-N-methylaniline → 3-(4-Tert-butyl-benzenesulfonylamino)-5-chloro-pyridine-2-carboxylic acid (2-fluoro-phenyl)-methyl-amide

https://huagongshe.com/ko/reaction/419207

반응식

참여 물질

역할이름HCID투입량
반응물2-Fluoro-N-methylanilineHCID 2759010—
반응물Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 9886157—
반응물3-(4-tert-Butyl-benzenesulfonylamino)-5-chloro-pyridine-2-carboxylic acidHCID 57942326—
용매N-methyl-2-pyrrolidoneHCID 13387—
생성물3-(4-Tert-butyl-benzenesulfonylamino)-5-chloro-pyridine-2-carboxylic acid (2-fluoro-phenyl)-methyl-amideHCID 57942551—

반응 조건

온도60 °C

반응 단계

3-(4-tert-Butyl-benzenesulfonylamino)-5-chloro-pyridine-2-carboxylic acid (75 mg, 0.20 mmol), (2-fluoro-phenyl)-methyl-amine (23 mg, 0.61 mmol), HATU (193 mg, 0.51 mmol), TEA (114 μL, 0.81 mmol) and 0.5 mL NMP were combined in a 4 mL vial and stirred overnight at 60° C. HPLC purification (10 to 95% gradient of MeCN-water) provided 3-(4-tert-butyl-benzenesulfonylamino)-5-chloro-pyridine-2-carboxylic acid (2-fluoro-phenyl)-methyl-amide: 1H NMR (400 MHz, CDCl3) 9.98 (s, 1H), 8.01 (s, 1H), 7.82 (d, 2H), 7.63 (s, 1H), 7.51 (d, 2H), 7.13 (m, 1H), 6.92 (t, 1H), 6.84 (t, 1H), 6.37 (m, 1H), 3.38 (t, 3H), 1.26 (s, 9H); MS m/z 476.1.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08093247B2
출처 데이터셋uspto-grants-2012_01
ORD IDord-b519375c03134063a05d213707f5675c
출처 메모uspto-grants-2012_01