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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 847생성일: 2026년 10월 23일

Ammonia → 2-Amino-6-(3-methoxy-5-methyl-phenyl)sulfonyl-benzonitrile

https://huagongshe.com/ko/reaction/847

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참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물6-Fluoro-2-[(3-methoxy-5-methylphenyl)sulfonyl]benzenecarbonitrileHCID 486358—
용매EthanolHCID 702—
용매TetrahydrofuranHCID 8028—
생성물2-Amino-6-(3-methoxy-5-methyl-phenyl)sulfonyl-benzonitrileHCID 48346434%

반응 조건

온도130 °C

반응 단계

A solution of 0.3 g (0.00098 mol) of 2-fluoro-6-[(3-methyl-5-methoxyphenyl)sulfonyl]benzonitrile (Example 25) in 10 mL of absolute ethanol and ca. 2 mL of THF was saturated with ammonia. The resultant solution was sealed in a glass-lined Parr bomb and heated to 130° C. for 4 h. The solvent was removed in vacuo. 20 mL of 1 NaOH was added. This aqueous solution was extracted with 3×50 mL of EtOAc. The EtOAc solution was dried over MgSO4. After solvent removal, the crude product was recrystallized from absolute ethanol to give 0.1 g (34%) of 2-amino-6-[(3-methyl-5-methoxyphenyl)sulfonyl]benzonitrile: mp 166°-168° C.; NMR (Me2SO-d6, 200 MHz δ 2.4 (s, 3H), 3.87 (s, 3H), 6.7 (br s, 2H), 7.13 (apparent d, 1H), 7.2 (unresolved s, 1H), 7.3-7.5 (m, 2H), 7.57 (apparent t, 1H). Anal. Calc. for C15H14N2O3S: C, 59.59; H, 4.67;N, 9.27; S, 10.6. Found: C, 59.67;H, 4.71;N, 9.25; S, 10.51.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US05723452
출처 데이터셋uspto-grants-1998_03
ORD IDord-b52dd58a1564476b8012385c8b071efd
출처 메모uspto-grants-1998_03