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Potassium Carbonate → 2-Ethyl-pyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl ester

HRID 549376
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인쇄 미리보기

반응식

HRID 549376 반응식
[I-].[NH2:2][N+:3]1[CH:8]=[CH:7][CH:6]=[CH:5][CH:4]=1.C(=O)([O-])[O-].[K+].[K+].[CH2:15]([O:17][C:18](=[O:23])[C:19]#[C:20][CH2:21][CH3:22])[CH3:16]>CN(C)C=O>[CH2:15]([O:17][C:18]([C:19]1[C:20]([CH2:21][CH3:22])=[N:2][N:3]2[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=12)=[O:23])[CH3:16]
참가 물질실험 절차후처리출처 및 근거반응 노트

참가 물질

5

반응물 3

HCID 11430Potassium CarbonateHCID 99169Ethyl pent-2-yn-1-oateHCID 2733704Pyridinium, 1-amino-, iodide (1:1)

생성물 1

HCID 137381512-Ethyl-pyrazolo[1,5-a]pyridine-3-carboxylic acid ethyl ester수율 55%

시약·촉매·용매 1

HCID 6228Dimethylformamide용매

실험 절차

To a solution of amino-pyridinium iodide (22 g, 99 mmol) and anhydrous potassium carbonate (17.8 g, 128.7 mmol) in dimethylformamide (225 mL) was added ethyl-2-pentynoate (24.98 g, 198 mmol). The solution was stirred at room temperature for 24 h. The reaction mixture was poured into 1.2 L of ice water. The resulting light brown precipitate was collected by vacuum filtration and air-dried for 16 h to yield crude product (1.9 g, 55%), which was used without further purification.

후처리

  1. filtrationThe resulting light brown precipitate was collected by vacuum filtration
  2. customair-dried for 16 h

출처 및 근거

ORD 기록
ord-0711d30d2b0d4855b0d8b6fa819b0502
출처 데이터셋
uspto-grants-2011_05
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US07943652B2

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