Hydrochloric Acid → (R)-2-(4-Fluoro-3,5-dimethyl-phenylamino)-hexanoic acid

HRID 885501

反応式

HRID 885501 の反応式
[NH2:1][C@H:2]([CH2:6][CH2:7][CH2:8][CH3:9])[C:3]([OH:5])=[O:4].Br[C:11]1[CH:12]=[C:13]([CH3:19])[C:14]([F:18])=[C:15]([CH3:17])[CH:16]=1.C([O-])([O-])=O.[K+].[K+].Cl>C(OCC)(=O)C.O.[Cu]I.CC(N(C)C)=O>[F:18][C:14]1[C:15]([CH3:17])=[CH:16][C:11]([NH:1][C@H:2]([CH2:6][CH2:7][CH2:8][CH3:9])[C:3]([OH:5])=[O:4])=[CH:12][C:13]=1[CH3:19]

参加物

9

反応条件

温度
90 °C

実験手順

(R)-2-Amino-hexanoic acid (0.840 g, 6.4 mmol), 5-bromo-2-fluoro-1,3-dimethyl-benzene (1.292 g, 6.4 mmol), CuI (0.122 g, 0.64 mmol), and K2CO3 (1.326 g, 9.6 mmol) were weighed into a Schlenk flask. To this was added 8 mL of dimethylacetamide and the resulting mixture vacuum-pumped and nitrogen-filled alternatively three times. After heating to 90° C. with stirring for 39 h, the reaction mixture was cooled to room temperature, diluted with 20 mL of ethyl acetate and 10 mL of water, and then acidified with concentrated HCl to pH=3. The layers were separated and the aqueous layer extracted with ethyl acetate (20 mL×5). The organic layers were combined and dried over anhydrous Na2SO4. Removal of the solvent under reduced pressure gave the title product which was used directly in the next step with further purification. LC-MS: tR=8.5 min, m/z 254 (M+H)+.

後処理

  1. additionthe resulting mixture vacuum-pumped and nitrogen-filled alternatively three times
  2. temperaturethe reaction mixture was cooled to room temperature
  3. customThe layers were separated
  4. extractionthe aqueous layer extracted with ethyl acetate (20 mL×5)
  5. dry with materialdried over anhydrous Na2SO4
  6. customRemoval of the solvent under reduced pressure

出典と根拠

ORDレコード
ord-fa77dd1252564d68b6b8a2dd1d36679e
出典データセット
uspto-grants-2012_08
特許番号
US08242174B2

関連ノート

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