Ammonia → 3-(4-(4-Fluorophenoxy)phenyl)propanimidamide

HRID 705841ノート

反応式

HRID 705841 の反応式
[F:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][C:15]#[N:16])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1.C(Cl)(C)=O.[NH3:23]>C1(C)C=CC=CC=1.CO>[F:1][C:2]1[CH:18]=[CH:17][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([CH2:13][CH2:14][C:15](=[NH:23])[NH2:16])=[CH:9][CH:8]=2)=[CH:4][CH:3]=1

参加物

6

実験手順

To a solution of 3-(4-(4-fluorophenoxyl)phenyl)propanenitrile (4.4 g, 18.24 mmol) in toluene (25 mL) and methanol (5.94 mL) was added dropwise AcCl (6.48 mL, 91 mmol) at 0° C. in 5 min. The mixture was stirred at room temperature for 2 h. The mixture was cooled to 0° C. in an ice bath, and ammonia (26.1 mL, 182 mmol) in methanol was added dropwise in 5 min. The mixture was stirred at room temperature overnight. The mixture was filtered to remove the solid, and the solid was washed with toluene (40 mL) and methanol (40 mL). The combined filtrate was concentrated in vacuo, the residue was triturated with diethyl ether, the resulting white solid was collected by filtration, washed with diethyl ether and dried in vacuo to afford the title compound (5.4 g, 16.12 mmol, 88% yield) as white solid. LCMS: rt=1.03 min, [M+H+]=259

後処理

  1. temperatureThe mixture was cooled to 0° C. in an ice bath
  2. stirringThe mixture was stirred at room temperature overnight
  3. filtrationThe mixture was filtered
  4. customto remove the solid
  5. washthe solid was washed with toluene (40 mL) and methanol (40 mL)
  6. concentrationThe combined filtrate was concentrated in vacuo
  7. customthe residue was triturated with diethyl ether
  8. filtrationthe resulting white solid was collected by filtration
  9. washwashed with diethyl ether
  10. customdried in vacuo

出典と根拠

ORDレコード
ord-82a3282461eb4ef2beefb9caf4a49083
出典データセット
uspto-grants-2015_11
特許番号
US09174968B2

反応ノート

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