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3-Pyridinecarboxaldehyde → Benzyl (E)-3-[2-methyl-3-(3-pyridylmethyl)-1H-indol-4-yl]-2-propenoate

HRID 1600175
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HRID 1600175 반응식
[CH3:1][C:2]1[NH:3][C:4]2[C:9]([CH:10]=1)=[C:8](/[CH:11]=[CH:12]/[C:13]([O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14])[CH:7]=[CH:6][CH:5]=2.[N:23]1[CH:28]=[CH:27][CH:26]=[C:25]([CH:29]=O)[CH:24]=1.C([SiH](CC)CC)C>ClCCl.FC(F)(F)C(O)=O>[CH3:1][C:2]1[NH:3][C:4]2[C:9]([C:10]=1[CH2:29][C:25]1[CH:24]=[N:23][CH:28]=[CH:27][CH:26]=1)=[C:8](/[CH:11]=[CH:12]/[C:13]([O:15][CH2:16][C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1)=[O:14])[CH:7]=[CH:6][CH:5]=2
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참가 물질

6

반응물 3

HCID 103713-PyridinecarboxaldehydeHCID 12052TriethylsilaneHCID 86752481Benzyl (E)-3-(2-methyl-1H-indol-4-yl)-2-propenoate

생성물 1

HCID 86752482Benzyl (E)-3-[2-methyl-3-(3-pyridylmethyl)-1H-indol-4-yl]-2-propenoate수율 35.1%

시약·촉매·용매 2

HCID 6344Dichloromethane용매
HCID 6422
Trifluoroacetic acid
용매

실험 절차

A solution of benzyl (E)-3-[2-methyl-1H-indol-4-yl]-2-propenoate (4.75 g) and pyridine-3-carboxaldehyde (2.10 g) in dry dichloromethane (45 ml) was added dropwise to a stirred solution of triethylsilane (7.82 ml) in trifluoroacetic acid (40 ml) at 0° C. The solution was stirred, allowing the temperature to rise to room temperature, for 45 minutes and then evaporated. The residue was partitioned between dichloromethane and dilute aqueous ammonia solution. The aqueous layer was extracted with dichloromethane, and the combined organic layers were washed with water and dried (MgSO4). The solvent was evaporated and the residue was chromatographed on silica gel. Elution with dichloromethane gave impurity,and further elution with dichloromethane/methanol (19:1) gave pure product.The product fractions were evaporated and the residue was triturated with ether to give the title compound (2.19 g), m.p. 180°-182° C., Rf. 0.35(SS1).

후처리

  1. customevaporated
  2. customThe residue was partitioned between dichloromethane and dilute aqueous ammonia solution
  3. extractionThe aqueous layer was extracted with dichloromethane
  4. washthe combined organic layers were washed with water
  5. dry with materialdried (MgSO4)
  6. customThe solvent was evaporated
  7. customthe residue was chromatographed on silica gel
  8. washElution with dichloromethane
  9. customgave
  10. washimpurity,and further elution with dichloromethane/methanol (19:1)
  11. customgave pure product.The product fractions
  12. customwere evaporated
  13. customthe residue was triturated with ether

출처 및 근거

ORD 기록
ord-d93c3fe558dd43198942a8b39f2c911c
출처 데이터셋
uspto-grants-1998_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US05744488

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