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Methanol → 2-[4-(Cyclopentylamino)-2-fluoro-phenyl]propionic acid

HRID 1506861
ノート
印刷プレビュー

反応式

HRID 1506861 の反応式
[NH2:1][C:2]1[CH:7]=[CH:6][C:5]([CH:8]([CH3:13])[C:9]([O:11]C)=[O:10])=[C:4]([F:14])[CH:3]=1.CO.[C:17]1(=O)[CH2:21][CH2:20][CH2:19][CH2:18]1.C([BH3-])#N.[Na+]>C(O)(=O)C>[CH:17]1([NH:1][C:2]2[CH:7]=[CH:6][C:5]([CH:8]([CH3:13])[C:9]([OH:11])=[O:10])=[C:4]([F:14])[CH:3]=2)[CH2:21][CH2:20][CH2:19][CH2:18]1
参加物実験手順後処理出典と根拠反応ノート

参加物

6

反応物 4

HCID 887MethanolHCID 8452CyclopentanoneHCID 5003444Sodium cyanoborohydrideHCID 13758005Methyl 2-(4-amino-2-fluorophenyl)propanoate

生成物 1

HCID 601555292-[4-(Cyclopentylamino)-2-fluoro-phenyl]propionic acid

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

To a solution of 1.50 g (7.6 mmol) of compound (7) in a solvent mixture of 10 mL of methanol and 0.2 mL of acetic acid, 1.4 mL (15.2 mmol) of cyclopentanone and 0.96 g (15.2 mmol) of sodium cyanoborohydride (NaBH3CN) were added. The obtained solution was stirred at room temperature for 12 hours. Next, the reaction mixture was dried under a vacuum and extracted with dichloromethane, followed by drying over anhydrous sodium sulfate and subsequent filtration. The filtrate was dried under a vacuum, and the residue was purified by silica gel chromatograph (n-hexane/ethyl acetate 3:2) to give a methyl ester of compound (11a). This compound was hydrolyzed with sodium hydroxide to give 1.09 g (yield 54%) of compound (11a) of interest as brown powder.

後処理

  1. additionwere added
  2. customNext, the reaction mixture was dried under a vacuum
  3. extractionextracted with dichloromethane
  4. dry with materialby drying over anhydrous sodium sulfate and subsequent filtration
  5. customThe filtrate was dried under a vacuum
  6. customthe residue was purified by silica gel chromatograph (n-hexane/ethyl acetate 3:2)

出典と根拠

ORDレコード
ord-9cfb8d3dc354402ba1a44fdd56676d93
出典データセット
uspto-grants-2015_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09221786B2

反応ノート

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