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1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimide → N-(4-(2-Aminopyridin-4-yloxy)-3-fluorophenyl)-2-fluoro-5-methylbenzamide

HRID 2237200
ノート
印刷プレビュー

反応式

HRID 2237200 の反応式
[CH:1](N(C(C)C)CC)(C)C.N[C:11]1[N:16]=[CH:15][N:14]=[C:13]([O:17][C:18]2[CH:23]=[CH:22][C:21]([NH:24]C(NC(=O)CC3C=CC(F)=CC=3)=S)=[CH:20][C:19]=2[F:38])[CH:12]=1.[F:39][C:40]1[CH:48]=[CH:47][C:46]([CH3:49])=[CH:45][C:41]=1[C:42]([OH:44])=O.CCN=C=NCCCN(C)C.C1C=CC2N(O)N=NC=2C=1>CN(C=O)C>[NH2:14][C:15]1[CH:1]=[C:13]([O:17][C:18]2[CH:23]=[CH:22][C:21]([NH:24][C:42](=[O:44])[C:41]3[CH:45]=[C:46]([CH3:49])[CH:47]=[CH:48][C:40]=3[F:39])=[CH:20][C:19]=2[F:38])[CH:12]=[CH:11][N:16]=1
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 5

HCID 159081-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 2428292-Fluoro-5-methylbenzoic acidHCID 115389121-(4-(6-Aminopyrimidin-4-yloxy)-3-fluorophenyl)-3-(2-(4-fluorophenyl)acetyl)thiourea2 回

生成物 1

HCID 59852870
N-(4-(2-Aminopyridin-4-yloxy)-3-fluorophenyl)-2-fluoro-5-methylbenzamide
収率 40%

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide溶媒

実験手順

Diisopropylethylamine (0.035 mL, 0.200 mmol, 2.0 eq) was added to a solution of 4-(4-amino-2-fluorophenoxy)pyridin-2-amine (Compound B of Example 24, 0.022 g, 0.100 mmol, 1.0 eq), 2-fluoro-5-methyl benzoic acid (Aldrich, 0.015 g, 0.100 mmol, 1.0 eq), EDCI (0.021 g, 0.11 mmol, 1.1 eq) and HOBT (0.014 g, 0.100 mmol, 1.0 eq) in DMF (0.700 mL) at room temperature. The reaction mixture was stirred at room temperature for 8 h, quenched with saturated aqueous NaHCO3 solution and extracted with CHCl3 (3×10 mL). The combined organic extracts were dried (Na2SO4), filtered and concentrated in vacuo. The residue was purified by reverse phase preparative HPLC (YMC ODS-A S10 30×500 mm, 30-90% aqueous MeOH with 0.1% TFA, 30 minute gradient) and the appropriate fractions were concentrated in vacuo. The concentrate was neutralized with saturated aqueous NaHCO3 solution and the mixture extracted with CHCl3 (3×30 mL). The combined organics were dried (Na2SO4), filtered and concentrated in vacuo to afford the title compound (0.014 g, 40%) as a solid. 1H NMR (CD3OD) δ 7.67-7.80 (m, 2H), 7.36-7.45 (m, 3H), 7.03-7.14 (m, 2H), 6.14-6.16 (m, 1H), 5.89-5.90 (m, 1H), 2.29 (s, 3H); MS(ESI+) m/z 356 (M+H)+; HRMS(ESI+) calcd.: 356.1211, found: 356.1203.

後処理

  1. customquenched with saturated aqueous NaHCO3 solution
  2. extractionextracted with CHCl3 (3×10 mL)
  3. dry with materialThe combined organic extracts were dried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customThe residue was purified by reverse phase preparative HPLC (YMC ODS-A S10 30×500 mm, 30-90% aqueous MeOH with 0.1% TFA, 30 minute gradient)
  7. concentrationthe appropriate fractions were concentrated in vacuo
  8. extractionthe mixture extracted with CHCl3 (3×30 mL)
  9. dry with materialThe combined organics were dried (Na2SO4)
  10. filtrationfiltered
  11. concentrationconcentrated in vacuo

出典と根拠

ORDレコード
ord-dd5a259f82094857a6a0e7b69db9a5f6
出典データセット
uspto-grants-2010_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07714138B2

反応ノート

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