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Water → 4-[1-(6-Bromopyridin-2-yl)-2-fluoroethyl]morpholine

HRID 385998
ノート
印刷プレビュー

反応式

HRID 385998 の反応式
[Br:1][C:2]1[CH:7]=[CH:6][CH:5]=[C:4]([CH:8](Br)[CH2:9][F:10])[N:3]=1.[NH:12]1[CH2:17][CH2:16][O:15][CH2:14][CH2:13]1.CCN(C(C)C)C(C)C.O>CN(C=O)C>[Br:1][C:2]1[N:3]=[C:4]([CH:8]([N:12]2[CH2:17][CH2:16][O:15][CH2:14][CH2:13]2)[CH2:9][F:10])[CH:5]=[CH:6][CH:7]=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 962WaterHCID 8083Morpholine2 回HCID 81531Diisopropylethylamine2 回HCID 595262542-Bromo-6-(1-bromo-2-fluoroethyl)pyridine

生成物 1

HCID 595261924-[1-(6-Bromopyridin-2-yl)-2-fluoroethyl]morpholine

試薬・触媒・溶媒 1

HCID 6228Dimethylformamide
溶媒

実験手順

2-Bromo-6-(1-bromo-2-fluoroethyl)pyridine (70 mg, 0.25 mmol), morpholine (0.022 mL, 0.25 mmol) and DIPEA (0.048 mL, 0.27 mmol) were stirred in DMF (1 mL) at room temperature for 4 hours. Additional morpholine (10.78 μL, 0.12 mmol) and DIPEA (0.024 mL, 0.14 mmol) were added and the resulting solution stirred at room temperature overnight. Water was added and the reaction mixture was extracted with EtOAc (2×). The combined organic extracts were washed with brine, dried over MgSO4, filtered, and concentrated in vacuo. Purification of the residue by silica gel column chromatography (6-50% EtOAc-hexanes) gave the title compound as a pale yellow oil.

後処理

  1. extractionthe reaction mixture was extracted with EtOAc (2×)
  2. washThe combined organic extracts were washed with brine
  3. dry with materialdried over MgSO4
  4. filtrationfiltered
  5. concentrationconcentrated in vacuo
  6. customPurification of the residue by silica gel column chromatography (6-50% EtOAc-hexanes)

出典と根拠

ORDレコード
ord-4f6bf62e0a944177b3b0a9192a4bfa16
出典データセット
uspto-grants-2013_02
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08367706B2

反応ノート

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