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Potassium Carbonate → HCID 58367548, 화합물

HRID 729481
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HRID 729481 반응식
Cl[C:2]1[N:3]=[CH:4][C:5]([C:8]([O:10][CH3:11])=[O:9])=[N:6][CH:7]=1.Cl.[Br:13][C:14]1[CH:24]=[CH:23][C:22]([F:25])=[CH:21][C:15]=1[O:16][CH:17]1[CH2:20][NH:19][CH2:18]1.C(=O)([O-])[O-].[K+].[K+]>O1CCOCC1>[Br:13][C:14]1[CH:24]=[CH:23][C:22]([F:25])=[CH:21][C:15]=1[O:16][CH:17]1[CH2:20][N:19]([C:2]2[N:3]=[CH:4][C:5]([C:8]([O:10][CH3:11])=[O:9])=[N:6][CH:7]=2)[CH2:18]1
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참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 406081Methyl 5-chloropyrazine-2-carboxylateHCID 67300218Azetidine, 3-(2-bromo-5-fluorophenoxy)-, hydrochloride (1:1)

생성물 1

HCID 58367548HCID 58367548, 화합물

시약·촉매·용매 1

HCID 312751,4-Dioxane용매

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온도
100 °C

실험 절차

To a mixture of methyl 5-chloropyrazine-2-carboxylate (0.47 g, 2.7 mmol), 3-(2-bromo-5-fluorophenoxy)azetidine hydrochloride salt (0.80 g, 3.2 mmol) and potassium carbonate (0.75 g, 5.42 mmol) in dioxane (13 mL) was heated at 100° C. After a period of 4 h, the reaction mixture was partitioned between ethyl acetate and saturated ammonium chloride. The organic phase was separated, dried over sodium sulfate, filtered and evaporated under reduced pressure. The resulting solid was taken in ether and filtered to give the title compound.

후처리

  1. customthe reaction mixture was partitioned between ethyl acetate and saturated ammonium chloride
  2. customThe organic phase was separated
  3. dry with materialdried over sodium sulfate
  4. filtrationfiltered
  5. customevaporated under reduced pressure
  6. filtrationfiltered

출처 및 근거

ORD 기록
ord-7f498345315d4f1f8831d0c245547db4
출처 데이터셋
uspto-grants-2009_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07582633B2

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