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4-Methyl-3-oxopentanenitrile → 3-isopropyl-1-(pyridin-3-yl)-1H-pyrazol-5-amine

HRID 631706
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HRID 631706 반응식
[CH3:1][CH:2]([CH3:8])[C:3](=O)[CH2:4][C:5]#[N:6].Cl.[NH:10]([C:12]1[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=1)[NH2:11]>CCO>[CH:2]([C:3]1[CH:4]=[C:5]([NH2:6])[N:10]([C:12]2[CH:13]=[N:14][CH:15]=[CH:16][CH:17]=2)[N:11]=1)([CH3:8])[CH3:1]
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참가 물질

4

반응물 2

HCID 101299214-Methyl-3-oxopentanenitrileHCID 231434543-Hydrazinylpyridine hydrochloride

생성물 1

HCID 668772093-isopropyl-1-(pyridin-3-yl)-1H-pyrazol-5-amine수율 32.8%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
80 °C

실험 절차

Using the procedure described in Example 308A Step 1, to a solution of 4-methyl-3-oxopentanenitrile (303 mg, 2.7 mmol) prepared as described in Example 122A Step 1, in anhydrous EtOH (13 ml) was added 3-hydrazinylpyridine hydrochloride (450 mg, 3.1 mmol) and the reaction mixture was heated at 80° C. overnight to afford 3-isopropyl-1-(pyridin-3-yl)-1H-pyrazol-5-amine (179 mg, 28%) as a solid. 1H NMR (300 MHz, CDCl3) δ 1.25 (d, J=7 Hz, 6H), 2.90-2.99 (m, 1H), 3.93 (brs, 2H), 5.50 (s, 1H), 7.36-7.38 (m, 1H), 7.96 (d, J=8 Hz, 1H), 8.49 (d, J=7 Hz, 1H), 8.67 (s, 1H); LC-MS (ESI) m/z 203 (M+H)+.

후처리

  1. customprepared

출처 및 근거

ORD 기록
ord-8081c6dfb3db4d9a890a7d6eb7d961c8
출처 데이터셋
uspto-grants-2016_04
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US09320739B2

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