반응 #943

ord-b52dd58a1564476b8012385c8b071efd

반응 방정식

COc1cc(C)cc(S(=O)(=O)c2cccc(F)c2C#N)c1
2-fluoro-6-[(3-methyl-5-methoxyphenyl)sulfonyl]benzonitrile
COc1cc(C)cc(S(=O)(=O)c2cccc(F)c2C#N)c1
2-Fluoro-6-[(3 -methyl-5-methoxyphenyl)sulfonyl]benzonitrile
N
ammonia
COc1cc(C)cc(S(=O)(=O)c2cccc(N)c2C#N)c1
2-amino-6-[(3-methyl-5-methoxyphenyl)sulfonyl]benzonitrile
수율 34.0%

반응 조건

온도
130°CELSIUS
상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타The solvent was removed in vacuo
  2. 2
    workup.ADDITION20 mL of 1 NaOH was added
  3. 3
    추출This aqueous solution was extracted with 3×50 mL of EtOAc
  4. 4
    건조The EtOAc solution was dried over MgSO4
  5. 5
    기타After solvent removal
  6. 6
    기타the crude product was recrystallized from absolute ethanol

실험 절차

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

DOI: 10.6084/m9.figshare.5104873.v1특허: US05723452uspto-grants-1998_03