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Potassium Carbonate → 1-(4-{4-[3-(1H-indol-5-yl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-benzyl}-piperazin-yl)-ethanone

HRID 85049
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HRID 85049 반응식
Br[CH2:2][C:3]1[CH:8]=[CH:7][C:6](B2OC(C)(C)C(C)(C)O2)=[CH:5][CH:4]=1.[C:18]([N:21]1[CH2:26][CH2:25][NH:24][CH2:23][CH2:22]1)(=[O:20])[CH3:19].C([O-])([O-])=O.[K+].[K+].Br[C:34]1[CH:35]=[C:36]2[C:42]([C:43]3[CH:44]=[C:45]4[C:49](=[CH:50][CH:51]=3)[NH:48][CH:47]=[CH:46]4)=[CH:41][N:40](S(C3C=CC(C)=CC=3)(=O)=O)[C:37]2=[N:38][CH:39]=1>CN(C=O)C.Cl[Pd](Cl)([P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1)[P](C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1>[NH:48]1[C:49]2[C:45](=[CH:44][C:43]([C:42]3[C:36]4[C:37](=[N:38][CH:39]=[C:34]([C:6]5[CH:5]=[CH:4][C:3]([CH2:2][N:24]6[CH2:25][CH2:26][N:21]([C:18](=[O:20])[CH3:19])[CH2:22][CH2:23]6)=[CH:8][CH:7]=5)[CH:35]=4)[NH:40][CH:41]=3)=[CH:51][CH:50]=2)[CH:46]=[CH:47]1
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참가 물질

7

반응물 4

HCID 11430Potassium CarbonateHCID 837951-AcetylpiperazineHCID 37345062-(4-(Bromomethyl)phenyl)-4,4,5,5-tetramethyl-1,3,2-dioxaborolaneHCID 667791765-bromo-3-(1H-indol-5-yl)-1-tosyl-1H-pyrrolo[2,3-b]pyridine

생성물 1

HCID 462360471-(4-{4-[3-(1H-indol-5-yl)-1H-pyrrolo[2,3-b]pyridin-5-yl]-benzyl}-piperazin-yl)-ethanone수율 46%

시약·촉매·용매 2

HCID 178418476HCID 178418476, 화합물촉매HCID 6228Dimethylformamide용매

실험 절차

2-(4-Bromomethyl-phenyl)-4,4,5,5-tetramethyl-[1,3,2]dioxaborolane (100 mg, 0.337 mmol), N-acetylpiperazine (47 mg, 0.37 mmol) and K2CO3 (93 mg, 0.675 mmol) were combined in DMF (2.5 ml) and stirred overnight at room temperature. The reaction was quenched by the addition of water, extracted with DCM and dried. The residue was taken up in CH3CN (2 ml), Intermediate B (120 mg, 0.275 mmol) and dichlorobis(triphenylphosphine)palladium (II) (10 mg, 0.013 mmol) were added and the reaction was heated to 150° C. in a microwave reactor for 20 min. The mixture was partitioned between water and DCM, the organic phase dried, evaporated and purified by silica gel chromatography using 0-5% MeOH:DCM. 53 mg (46%) of the title compound were obtained. MS ESI (m/z): 450.4 (M+1)+, calc. 449.

후처리

  1. customThe reaction was quenched by the addition of water
  2. extractionextracted with DCM
  3. customdried
  4. temperaturethe reaction was heated to 150° C. in a microwave reactor for 20 min
  5. customThe mixture was partitioned between water and DCM
  6. customthe organic phase dried
  7. customevaporated
  8. custompurified by silica gel chromatography

출처 및 근거

ORD 기록
ord-89b44f887961403bb9b41854013c0a0f
출처 데이터셋
uspto-grants-2014_09
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08846909B2

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