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

HRID 1026743
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HRID 1026743 반응식
[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
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

6

반응물 4

HCID 6363IsopropylamineHCID 516892Sodium BicarbonateHCID 27629912-Bromo-4-pyridinecarboxaldehydeHCID 5049666Sodium triacetoxyborohydride

생성물 1

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

시약·촉매·용매 1

HCID 6212Chloroform용매

실험 절차

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).

후처리

  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)

출처 및 근거

ORD 기록
ord-5846bd16d3c644b6aeb1132c4549306e
출처 데이터셋
uspto-grants-2014_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08729271B2

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