Sodium Hydroxide → 6-Bromo-2-pyrrolidin-1-ylmethyl-1,2,3,4-tetrahydro-quinoline

HRID 1916630ノート

反応式

HRID 1916630 の反応式
[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[N:8]=[C:7]([CH2:12][N:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1)[CH:6]=[CH:5]2.[OH-].[Na+]>C(O)(=O)C>[Br:1][C:2]1[CH:3]=[C:4]2[C:9](=[CH:10][CH:11]=1)[NH:8][CH:7]([CH2:12][N:13]1[CH2:17][CH2:16][CH2:15][CH2:14]1)[CH2:6][CH2:5]2

参加物

4

反応物 2

HCID 14798Sodium HydroxideHCID 673647966-Bromo-2-pyrrolidin-1-ylmethyl-quinoline

生成物 1

HCID 673633166-Bromo-2-pyrrolidin-1-ylmethyl-1,2,3,4-tetrahydro-quinoline

試薬・触媒・溶媒 1

HCID 176Acetic Acid溶媒

実験手順

Under an argon atmosphere 0.69 mL (6.87 mmol) borane-pyridine complex are added to a solution of 500 mg (1.72 mmol) 6-bromo-2-pyrrolidin-1-ylmethyl-quinoline (see 3.45b) in 10 mL acetic acid at RT. The mixture is stirred for 7 h at RT, again combined with 0.35 mL (3.46 mmol) borane-pyridine complex and stirred for another hour at RT. It is cooled to 0° C. and the solution is made basic with 8% NaOH solution. The aqueous phase is extracted with EtOAc and the solvent is eliminated i.vac. The residue is taken up with water and acidified with 12% HCl. The aqueous phase is extracted with EtOAc and then made basic with 20% NaOH solution while cooling with ice. The aqueous phase is extracted with EtOAc. The organic phase is dried over MgSO4 and the solvent is eliminated i.vac.

後処理

  1. stirringstirred for another hour at RT
  2. temperatureIt is cooled to 0° C.
  3. extractionThe aqueous phase is extracted with EtOAc
  4. extractionThe aqueous phase is extracted with EtOAc
  5. temperaturewhile cooling with ice
  6. extractionThe aqueous phase is extracted with EtOAc
  7. dry with materialThe organic phase is dried over MgSO4

出典と根拠

ORDレコード
ord-e55d78a83c084218aa02717ed7bdf9d0
出典データセット
uspto-grants-2013_12
特許番号
US08618132B2

反応ノート

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