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Isopropylamine → 2-(Isopropylamino)-6-methoxyquinoline-3-carbaldehyde

HRID 1620214
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HRID 1620214 반응식
Cl[C:2]1[C:11]([CH:12]=[O:13])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([O:14][CH3:15])[CH:8]=2)[N:3]=1.[CH3:16][CH:17]([NH2:19])[CH3:18]>C1COCC1>[CH:17]([NH:19][C:2]1[C:11]([CH:12]=[O:13])=[CH:10][C:9]2[C:4](=[CH:5][CH:6]=[C:7]([O:14][CH3:15])[CH:8]=2)[N:3]=1)([CH3:18])[CH3:16]
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참가 물질

4

반응물 2

HCID 6363IsopropylamineHCID 6890792-Chloro-6-methoxyquinoline-3-carbaldehyde

생성물 1

HCID 866698202-(Isopropylamino)-6-methoxyquinoline-3-carbaldehyde수율 99.2%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

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온도
180 °C

실험 절차

To a stirred solution of 2-chloro-6-methoxyquinoline-3-carbaldehyde (1.50 g, 6.77 mmol) in THF (10 mL) in a 20 mL microwave vial equipped with a magnetic stirrer was added propan-2-amine (5.76 mL, 67.7 mmol) and the reaction mixture was stirred for 12.5 h at 160° C. and finally 45 min at 180° C. under microwave irradiation. After cooling to RT, the volatiles were removed at 40° C. under vacuum and the resulting yellow oil was taken up in a mixture of THF:1 N aq. HCl=1:1 (50 mL) and stirred for 1 h at RT. The volatiles were then removed at 40° C. under vacuum and the residue was then neutralised with saturated NaHCO3 aqueous solution before extraction with CH2Cl2 (100 mL). The organic phase was washed with brine (20 mL), dried over MgSO4, filtered, and concentrated under vacuum to give 2-(isopropylamino)-6-methoxyquinoline-3-carbaldehyde SLA 28186 as an orange solid (1.64 g, 99% yield).

후처리

  1. temperatureAfter cooling to RT
  2. customthe volatiles were removed at 40° C. under vacuum
  3. additionthe resulting yellow oil was taken up in a mixture of THF
  4. stirring1 N aq. HCl=1:1 (50 mL) and stirred for 1 h at RT
  5. customThe volatiles were then removed at 40° C. under vacuum
  6. extractionthe residue was then neutralised with saturated NaHCO3 aqueous solution before extraction with CH2Cl2 (100 mL)
  7. washThe organic phase was washed with brine (20 mL)
  8. dry with materialdried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated under vacuum

출처 및 근거

ORD 기록
ord-dc19ab3fbd3d42e6bca1d26efc49848f
출처 데이터셋
uspto-grants-2014_07
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08772316B2

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