Pyridine → HCID 54164588、化合物

HRID 369737ノート

反応式

HRID 369737 の反応式
[NH2:1][C:2]1[C:7]([C:8]([OH:18])([C:13]#[C:14]C(C)C)[C:9]([F:12])([F:11])[F:10])=[CH:6][C:5]([F:19])=[CH:4][CH:3]=1.N1[CH:25]=[CH:24]C=CC=1.Br[CH2:27][C:28](Br)=[O:29].[CH3:31]COCC>>[F:19][C:5]1[CH:4]=[CH:3][C:2]2[N:1]([C:24]#[CH:25])[C:28](=[O:29])[CH2:27][O:18][C:8]([CH:13]([CH3:14])[CH3:31])([C:9]([F:10])([F:11])[F:12])[C:7]=2[CH:6]=1

参加物

5

反応物 4

HCID 1049PyridineHCID 3283Diethyl Ether2 回HCID 61147Bromoacetyl bromideHCID 69959296HCID 69959296、化合物

生成物 1

HCID 54164588HCID 54164588、化合物

実験手順

To a stirred 0° solution of 210 mg of 6-Amino-3-fluoro-α-isopropylethynyl-α-(trifluoromEthyl)benzyl alcohol in 20 mL of dry ether was added 120 mL of dry pyridine and 0.080 mL of bromoacetyl bromide. After 30 min, the reaction mixture was diluted with ether, washed with water and aqueous sodium bicarbonate, dried and evaporated. The residue was dissolved in 20 mL of dry DMF and was treated at room temperature with 33 mg of 100% sodium hydride for 30 min. The reaction was partitioned between ethyl acetate and water and the ethyl acetate layer was washed with brine, dried and evaporated. The crude product was purified by column chromatography over silica gel (elution with ethyl acetate/hexanes 1:2) affording after crystallization from ethyl acetate/hexanes 89 mg of the title compound as colorless crystals: mp 172-173°; Anal. Calcd. for C15H13NO2F4 : C, 57.15; H, 4.17; N, 4.44. Found: C, 57.10; H, 3.98; N, 4.21.

後処理

  1. washwashed with water and aqueous sodium bicarbonate
  2. customdried
  3. customevaporated
  4. dissolutionThe residue was dissolved in 20 mL of dry DMF
  5. additionwas treated at room temperature with 33 mg of 100% sodium hydride for 30 min
  6. customThe reaction was partitioned between ethyl acetate and water
  7. washthe ethyl acetate layer was washed with brine
  8. customdried
  9. customevaporated
  10. customThe crude product was purified by column chromatography over silica gel (elution with ethyl acetate/hexanes 1:2)
  11. customaffording
  12. customafter crystallization from ethyl acetate/hexanes 89 mg of the title compound as colorless crystals

出典と根拠

ORDレコード
ord-e3de1fde1cb546a0955d66bed314b416
出典データセット
uspto-grants-2000_10
特許番号
US06140320

反応ノート

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