Water → HCID 10138368、化合物

HRID 2218465ノート

反応式

HRID 2218465 の反応式
C([Si](C)(C)[O:6][CH2:7][CH2:8][CH2:9][O:10][NH:11][C:12](=[O:29])[C:13]1[CH:18]=[CH:17][C:16]([F:19])=[CH:15][C:14]=1[NH:20][C:21]1[CH:26]=[CH:25][C:24]([I:27])=[CH:23][C:22]=1[CH3:28])(C)(C)C.OS(O)(=O)=O.C([O-])(O)=O.[Na+].O>CO>[F:19][C:16]1[CH:17]=[CH:18][C:13]([C:12]([NH:11][O:10][CH2:9][CH2:8][CH2:7][OH:6])=[O:29])=[C:14]([NH:20][C:21]2[CH:26]=[CH:25][C:24]([I:27])=[CH:23][C:22]=2[CH3:28])[CH:15]=1

参加物

6

反応物 4

HCID 962WaterHCID 1118Sulfuric Acid2 回HCID 516892Sodium BicarbonateHCID 22286093HCID 22286093、化合物

生成物 1

HCID 10138368HCID 10138368、化合物収率 74.3%

試薬・触媒・溶媒 1

HCID 887Methanol溶媒3 回

実験手順

To a solution of N-[3-(tert-Butyl-dimethyl-silanyloxy)-propoxy]-4-fluoro-2-(4-iodo-2-methyl-phenylamino)-benzamide (4.0 g, 7.27 mmol) in methanol (5 mL) at ambient temperature was added 5 M H2SO4 in methanol (0.073 mL, 0.364 mmol). After 1 h of stirring, to the reaction was added additional 5 M H2SO4 in methanol (0.035 mL, 0.182 mmol). After 2 h of stirring, the reaction was adjusted to pH 7 using saturated NaHCO3 (aq) (c.a. 1.5 mL), followed by addition of water (35 mL). The aqueous layer was extracted with ethyl acetate (1×20 mL, 2×10 mL). The extracts were combined, washed with brine, and dried over magnesium sulfate. The resultant mixture was filtered, and the filtrate solvent was removed in vacuo to obtain an oil that was dried on a vacuum pump over the weekend. The oil was purified by flash chromatography, eluted with a gradient of 100% hexanes to 100% ethyl acetate in 50 min. The solvent was removed in vacuo of combined fractions to obtain a solid which was dried on a vacuum pump for c.a. 6 h. Recrystalized solid in a mixture of hexanes and ethyl acetate to afford 4-fluoro-N-(3-hydroxy-propoxy)-2-(4-iodo-2-methyl-phenylamino)-benzamide as a solid (2.4 g, 74% yield): m.p. 120.8-122.4 C; 1H-NMR (400 MHz, (CD3)2CO) δ 10.91 (br s, 1H), 9.59 (br. S, 1H), 9.68 (m, 2H), 7.57 (d, 1H, J=8.54 Hz), 7.18 (d, 1H, J=8.34 Hz), 6.72 (m, 1H); 6.53 (m, 1H); 4.12 (t, 2H, J=6.11 Hz), 3.71 (t, 2H, J=5.86 Hz), 2.26 (s, 3H), 1.86 (m, 2H); 19F-NMR (376 MHz, (CD3)2CO) δ −108.14; MS 445.1 m/z (AP+), 443.1 m/z (AP−). Anal. Calcd. for C17H18FIN2O3: C, 45.96; H, 4.08; N, 6.31; F, 4.28; I, 28.57. Found: C, 45.78; H, 3.88; N, 6.14; F, 4.30; I, 28.27.

後処理

  1. stirringAfter 2 h of stirring
  2. extractionThe aqueous layer was extracted with ethyl acetate (1×20 mL, 2×10 mL)
  3. washwashed with brine
  4. dry with materialdried over magnesium sulfate
  5. filtrationThe resultant mixture was filtered
  6. customthe filtrate solvent was removed in vacuo
  7. customto obtain an oil that
  8. customwas dried on a vacuum pump over the weekend
  9. customThe oil was purified by flash chromatography
  10. washeluted with a gradient of 100% hexanes to 100% ethyl acetate in 50 min
  11. customThe solvent was removed in vacuo of combined fractions
  12. customto obtain a solid which
  13. customwas dried on a vacuum pump for c.a
  14. custom6 h
  15. customRecrystalized solid
  16. additionin a mixture of hexanes and ethyl acetate

出典と根拠

ORDレコード
ord-c325d22cf35b489ba03052a3d8441100
出典データセット
uspto-grants-2008_08
特許番号
US07411001B2

反応ノート

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