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Phenylhydrazine hydrochloride → 3-(1-Methylethyl)-1-phenyl-1H-pyrazol-5-amine

HRID 871719
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HRID 871719 반응식
[CH3:1][CH:2]([CH3:8])[C:3](=O)[CH2:4][C:5]#[N:6].Cl.[C:10]1([NH:16][NH2:17])[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1>CCO>[CH:2]([C:3]1[CH:4]=[C:5]([NH2:6])[N:16]([C:10]2[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=2)[N:17]=1)([CH3:8])[CH3:1]
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참가 물질

4

반응물 2

HCID 60962Phenylhydrazine hydrochlorideHCID 101299214-Methyl-3-oxopentanenitrile

생성물 1

HCID 27595063-(1-Methylethyl)-1-phenyl-1H-pyrazol-5-amine수율 77.8%

시약·촉매·용매 1

HCID 702Ethanol용매

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온도
65 °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 (6 ml) was added phenylhydrazine hydrochloride (473 mg, 3.3 mmol) and the reaction mixture was heated at 65° C. overnight. The residue was purified by silica gel chromatography (hexane/ethyl acetate 2-50%) to afford 3-isopropyl-1-phenyl-1H-pyrazol-5-amine (423 mg, 77%) as a solid. 1H NMR (300 MHz, CDCl3) δ 1.22 (d, J=6 Hz, 6H), 3.86 (brs, 2H), 5.35 (s, 1H), 7.21-7.49 (m, 5H); LC-MS (ESI) m/z 202 (M+H)+.

후처리

  1. customprepared
  2. customThe residue was purified by silica gel chromatography (hexane/ethyl acetate 2-50%)

출처 및 근거

ORD 기록
ord-3dec57124ec849eb8ac0273bee908dd6
출처 데이터셋
uspto-grants-2015_03
DOI
10.6084/m9.figshare.5104873.v1
특허 번호
US08969587B2

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