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Ammonium Chloride → 4-phenethyl-7H-pyrrolo[2,3-d]pyrimidine

HRID 552775
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HRID 552775 반응식
[CH2:1]([Mg]Br)[CH2:2][C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.Cl[C:12]1[C:13]2[CH:20]=[CH:19][NH:18][C:14]=2[N:15]=[CH:16][N:17]=1.[NH4+].[Cl-]>C1COCC1>[C:3]1([CH2:2][CH2:1][C:12]2[C:13]3[CH:20]=[CH:19][NH:18][C:14]=3[N:15]=[CH:16][N:17]=2)[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 25517Ammonium ChlorideHCID 53566827H-Pyrrolo(2,3-d)pyrimidine, 4-chloro-HCID 178419670HCID 178419670, 화합물

생성물 1

HCID 671649194-phenethyl-7H-pyrrolo[2,3-d]pyrimidine수율 54.3%

시약·촉매·용매 1

HCID 8028Tetrahydrofuran용매

실험 절차

Phenethyl magnesium bromide (0.5 M solution in THF, 12 mL, 6.15 mmol) was added dropwise to a stirred solution of 4-chloro-7H-pyrrolo[2,3-d]pyrimidine (0.210 g, 1.37 mmol) and Fe(acac)3 (0.1 g 0.273 mmol) in THF (5.0 mL) under Ar. The resulting reaction mixture was stirred at r.t. for 8 h. The mixture was poured onto a mixture of ice (10 mL) and NH4Cl (0.5 g) and the product was extracted with CHCl3. The combined organics were dried (Na2SO4), filtered and concentrated. The crude product was purified by flash chromatography (0 to 10% MeOH/DCM) to afford the title compound (0.166 g, 54%).

후처리

  1. customThe resulting reaction mixture
  2. extractionthe product was extracted with CHCl3
  3. dry with materialThe combined organics were dried (Na2SO4)
  4. filtrationfiltered
  5. concentrationconcentrated
  6. customThe crude product was purified by flash chromatography (0 to 10% MeOH/DCM)

출처 및 근거

ORD 기록
ord-cb1130a9fd9c4e1284fc08e6916e4e7e
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07951810B2

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