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Acetone → HCID 178457142, 화합물

HRID 1913553
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HRID 1913553 반응식
[C:1]1([C:7]2[N:8]=[C:9]([CH:12]([NH2:14])[CH3:13])[NH:10][CH:11]=2)[CH:6]=[CH:5][CH:4]=[CH:3][CH:2]=1.[CH3:15][C:16]([CH3:18])=O.[BH-](OC(C)=O)(OC(C)=O)OC(C)=O.[Na+]>ClCCCl>[CH:16]([NH:14][CH:12]([C:9]1[NH:10][CH:11]=[C:7]([C:1]2[CH:2]=[CH:3][CH:4]=[CH:5][CH:6]=2)[N:8]=1)[CH3:13])([CH3:18])[CH3:15]
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참가 물질

5

반응물 3

HCID 180AcetoneHCID 5049666Sodium triacetoxyborohydrideHCID 178463402HCID 178463402, 화합물

생성물 1

HCID 178457142HCID 178457142, 화합물수율 100%

시약·촉매·용매 1

HCID 111,2-Dichloroethane용매

실험 절차

1-(4-Phenyl-1H-imidazol-2-yl)-ethylamine (0.20 g, 1.07 mmol) and acetone (0.062 g, 1.07 mmol) were mixed in 1,2-dichloroethane (4 mL), followed by the addition of NaBH(OAc)3 (0.34 g, 1.61 mmol). The resulting mixture was stirred at rt for 3 h. The reaction was quenched with saturated NaHCO3 solution. The mixture was extracted with EtOAc and the combined extracts were dried over Na2SO4. Filtration followed by evaporation to dryness under reduced pressure gave the crude isopropyl-[1-(4-phenyl-1H-imidazol-2-yl)-ethyl]-amine (0.23 g, 100%) which was used for the next reaction without further purification. 1H NMR (300 MHz, CDCl3): δ 1.10 (3H, d), 1.18 (3H, d), 1.57 (3H, d), 2.86 (1H, m), 4.32 (1H, m), 7.24 (2H, m), 7.36 (2H, m), 7.69 (2H, m). MS (ES+): 230.2 (100%).

후처리

  1. customThe reaction was quenched with saturated NaHCO3 solution
  2. extractionThe mixture was extracted with EtOAc
  3. dry with materialthe combined extracts were dried over Na2SO4
  4. filtrationFiltration
  5. customfollowed by evaporation to dryness under reduced pressure

출처 및 근거

ORD 기록
ord-dad6aad7bdba420bbe184f738127c18e
출처 데이터셋
uspto-grants-2013_12
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08609709B2

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