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Sodium borohydride → HCID 21075807, 화합물

HRID 1373895
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HRID 1373895 반응식
[C:1](=[N:4][N:5]1[C:17]2[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=[CH:9][C:8]=2[N:7]=[C:6]1[CH3:18])([CH3:3])[CH3:2].[BH4-].[Na+]>CO>[CH:1]([NH:4][N:5]1[C:17]2[C:16]3[CH:15]=[CH:14][CH:13]=[CH:12][C:11]=3[N:10]=[CH:9][C:8]=2[N:7]=[C:6]1[CH3:18])([CH3:3])[CH3:2]
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참가 물질

4

반응물 2

HCID 4311764Sodium borohydrideHCID 21075811HCID 21075811, 화합물

생성물 1

HCID 21075807HCID 21075807, 화합물수율 100.2%

시약·촉매·용매 1

HCID 887Methanol용매

실험 절차

A solution of N-isopropylidene(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)amine (1.82 g, 7.64 mmol) dissolved in 40 mL of MeOH was treated with NaBH4 (1.16 g, 30.6 mmol). After stirring for 18 h, the reaction was quenched with saturated NH4Cl solution and partitioned between CH2Cl2 and 2% Na2CO3 solution. The organic portion was washed with 2% Na2CO3 solution, H2O and brine and dried over Na2SO4. The resulting organic portion was filtered and concentrated under reduced pressure to give N-isopropyl(2-methyl-1H-imidazo[4,5-c]quinolin-1-yl)amine (1.84 g) as a yellow foam.

후처리

  1. customthe reaction was quenched with saturated NH4Cl solution
  2. custompartitioned between CH2Cl2 and 2% Na2CO3 solution
  3. washThe organic portion was washed with 2% Na2CO3 solution, H2O and brine
  4. dry with materialdried over Na2SO4
  5. filtrationThe resulting organic portion was filtered
  6. concentrationconcentrated under reduced pressure

출처 및 근거

ORD 기록
ord-8c65c9cc8f5c4e89a42f0ed34fb7c749
출처 데이터셋
uspto-grants-2007_01
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07163947B2

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