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Water → (1-Pyrrolo[2,3-b]pyridin-1-yl-cyclopentyl)-acetonitrile

HRID 2169430
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HRID 2169430 반응식
[N:1]1([C:10]2([CH2:15][C:16]([NH2:18])=O)[CH2:14][CH2:13][CH2:12][CH2:11]2)[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[CH:2]1.N1C(Cl)=NC(Cl)=NC=1Cl.C(OCC)(=O)C.O>CN(C)C=O.CCCCCC>[N:1]1([C:10]2([CH2:15][C:16]#[N:18])[CH2:14][CH2:13][CH2:12][CH2:11]2)[C:5]2=[N:6][CH:7]=[CH:8][CH:9]=[C:4]2[CH:3]=[CH:2]1
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참가 물질

7

반응물 4

HCID 962WaterHCID 7954Cyanuric chlorideHCID 8857Ethyl AcetateHCID 867260602-(1-Pyrrolo[2,3-b]pyridin-1-yl-cyclopentyl)acetamide

생성물 1

HCID 86726061(1-Pyrrolo[2,3-b]pyridin-1-yl-cyclopentyl)-acetonitrile수율 58.1%

시약·촉매·용매 2

HCID 6228
Dimethylformamide
용매
HCID 8058Hexane용매

실험 절차

To a stirred solution of 2-(1-pyrrolo[2,3-b]pyridin-1-yl-cyclopentyl)-acetamide (398) (1.6 g, 6.58 mmol) in dimethylformamide (25 mL) was added cyanuric chloride (728 mg, 3.95 mmol) at room temperature. The reaction mixture was stirred for 30 min at room temperature (TLC, 30% ethyl acetate in hexane, Rf=0.8). Cold water was added and the mixture was extracted with ethyl acetate (2×50 mL) and washed with water (2×50 mL) and brine (50 mL). The organic phase was thereafter dried and concentrated to get a crude product. The crude product was purified by Combi-Flash column (eluted at 10-20% ethyl acetate in hexane) to get (1-pyrrolo[2,3-b]pyridin-1-yl-cyclopentyl)-acetonitrile (399) (861 mg, 58%) as a light yellow thick oil.

후처리

  1. extractionthe mixture was extracted with ethyl acetate (2×50 mL)
  2. washwashed with water (2×50 mL) and brine (50 mL)
  3. customThe organic phase was thereafter dried
  4. concentrationconcentrated
  5. customto get a crude product
  6. customThe crude product was purified by Combi-Flash column (eluted at 10-20% ethyl acetate in hexane)

출처 및 근거

ORD 기록
ord-6880419386004c759e5009f708717246
출처 데이터셋
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09045486B2

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