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Isopropylamine → N-[(2-Bromopyridin-4-yl)methyl]propan-2-amine

HRID 1026743
ノート
印刷プレビュー

反応式

HRID 1026743 の反応式
[CH:1]([NH2:4])([CH3:3])[CH3:2].[Br:5][C:6]1[CH:11]=[C:10]([CH:12]=O)[CH:9]=[CH:8][N:7]=1.C(O[BH-](OC(=O)C)OC(=O)C)(=O)C.[Na+].C(=O)([O-])O.[Na+]>C(Cl)(Cl)Cl>[Br:5][C:6]1[CH:11]=[C:10]([CH2:12][NH:4][CH:1]([CH3:3])[CH3:2])[CH:9]=[CH:8][N: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 6363IsopropylamineHCID 516892Sodium BicarbonateHCID 27629912-Bromo-4-pyridinecarboxaldehydeHCID 5049666Sodium triacetoxyborohydride

生成物 1

HCID 53385538N-[(2-Bromopyridin-4-yl)methyl]propan-2-amine

試薬・触媒・溶媒 1

HCID 6212Chloroform溶媒

実験手順

After a mixture of isopropylamine (2.8 mL), 2-bromopyridine-4-carboxaldehyde (3.00 g), and chloroform (60 mL) was stirred at room temperature, sodium triacetoxyborohydride (10.00 g) was added thereto and the mixture was stirred for 21 hr. Saturated aqueous sodium hydrogen carbonate solution was added to the reaction mixture, and the resulting mixture was then stirred for a while and extracted with chloroform. The organic phase was separated out and the solvent was distilled off under reduced pressure. The resulting residue was purified by column chromatography (silica gel cartridge, hexane:ethyl acetate=88:12-0:100) and (NH silica gel cartridge, hexane:ethyl acetate=90:10-0:100) to afford the title compound (2.64 g).

後処理

  1. stirringthe mixture was stirred for 21 hr
  2. stirringthe resulting mixture was then stirred for a while
  3. extractionextracted with chloroform
  4. customThe organic phase was separated out
  5. distillationthe solvent was distilled off under reduced pressure
  6. customThe resulting residue was purified by column chromatography (silica gel cartridge, hexane:ethyl acetate=88:12-0:100) and (NH silica gel cartridge, hexane:ethyl acetate=90:10-0:100)

出典と根拠

ORDレコード
ord-5846bd16d3c644b6aeb1132c4549306e
出典データセット
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US08729271B2

反応ノート

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