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

HRID 2169430
ノート
印刷プレビュー

反応式

HRID 2169430 の反応式
[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
参加物実験手順後処理出典と根拠反応ノート

参加物

7

反応物 4

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

生成物 1

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

試薬・触媒・溶媒 2

HCID 6228Dimethylformamide
溶媒
HCID 8058Hexane溶媒

実験手順

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.

後処理

  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)

出典と根拠

ORDレコード
ord-6880419386004c759e5009f708717246
出典データセット
uspto-grants-2015_06
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US09045486B2

反応ノート

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