تفاعل #942

ord-1a88c0d5212446d3b4c2d1662ded1557

معادلة التفاعل

COc1cc(C)cc(Sc2cccc(F)c2C#N)c1
2-fluoro-6-[(3-methyl-5-methoxyphenyl)thio]benzonitrile
COc1cc(C)cc(Sc2cccc(F)c2C#N)c1
2-Fluoro-6-[(3 -methyl-5-methoxyphenyl)thio]benzonitrile
N
ammonia
COc1cc(C)cc(Sc2cccc(N)c2C#N)c1
2-Amino-6-[(3 -methyl-5-methoxyphenyl)thio]benzonitrile

المذيبات

ظروف التفاعل

درجة الحرارة
145°CELSIUS
الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىThe solvent was removed in vacuo
  2. 2
    workup.ADDITION20 mL of 1 NaOH was added
  3. 3
    استخلاصThis aqueous solution was extracted with 3×20 mL of EtOAc
  4. 4
    تجفيفThe EtOAc solution was dried over MgSO4
  5. 5
    أخرىAfter solvent removal
  6. 6
    أخرىthe crude product was chromatographed on silica gel (flash; CH2Cl2)
  7. 7
    أخرىresulting in 0.03 g (30%) of 2-amino-6-[(3-methyl-5-methoxyphenyl)thio]benzonitrile as a white solid

الإجراء التجريبي

A solution of 0.1 g (0.00037 mol) of 2-fluoro-6-[(3-methyl-5-methoxyphenyl)thio]benzonitrile (Example 23) 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 145° C. for 48 h. The solvent was removed in vacuo. 20 mL of 1 NaOH was added. This aqueous solution was extracted with 3×20 mL of EtOAc. The EtOAc solution was dried over MgSO4. After solvent removal, the crude product was chromatographed on silica gel (flash; CH2Cl2), resulting in 0.03 g (30%) of 2-amino-6-[(3-methyl-5-methoxyphenyl)thio]benzonitrile as a white solid: mp 108°-110° C.; NMR (Me2SO-d6, 200 MHz) δ 2.32 (s, 3H), 3.78 (s, 3H), 6.28 (br s, 1H), 6.4 (apparent d, 1H), 6.7-6.8 (m, 2H), 6.8-6.9 (narrow m, 2H), 7.28 (apparent d, H). Anal. Calc. for C15H14N2OS: C, 66.64; H, 5.22; N, 10.36; S, 11.36. Found: C, 66.46; H, 5.22; N, 10.25; S, 11.71.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US05723452uspto-grants-1998_03