Ethyl 2-[(2'-cyanobiphenyl-4-yl)methyl]-3-oxohexanoate → 4'-{[2-(Methoxymethyl)-4-(1-methylpropyl)-5-oxo-7-propyl-4,5-dihydro[1,2,4]triazolo[1,5-a]pyrimidin-6-yl]methyl}biphenyl-2-carbonitrile

HRID 519503노트

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HRID 519503 반응식
[C:1]([C:3]1[CH:8]=[CH:7][CH:6]=[CH:5][C:4]=1[C:9]1[CH:14]=[CH:13][C:12]([CH2:15][CH:16]([C:22](=O)[CH2:23][CH2:24][CH3:25])[C:17](OCC)=[O:18])=[CH:11][CH:10]=1)#[N:2].[CH3:27][O:28][CH2:29][C:30]1[NH:31][C:32]([NH:35][CH:36]([CH3:39])[CH2:37][CH3:38])=[N:33][N:34]=1>>[CH3:27][O:28][CH2:29][C:30]1[N:31]=[C:32]2[N:35]([CH:36]([CH3:39])[CH2:37][CH3:38])[C:17](=[O:18])[C:16]([CH2:15][C:12]3[CH:13]=[CH:14][C:9]([C:4]4[C:3]([C:1]#[N:2])=[CH:8][CH:7]=[CH:6][CH:5]=4)=[CH:10][CH:11]=3)=[C:22]([CH2:23][CH2:24][CH3:25])[N:33]2[N:34]=1

참가 물질

3

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온도
250 °C

실험 절차

A mixture of ethyl 2-[(2′-cyanobiphenyl-4-yl)methyl]-3-oxohexanoate (0.75 g) and 5-(methoxymethyl)-N-(1-methylpropyl)-4H-1,2,4-triazol-3-amine (0.2 g) was stirred at 250° C. for 15 min under microwave irradiation. The obtained reaction mixture was purified by silica gel column chromatography to give the title compound as a colorless solid (0.2 g, 41%).

후처리

  1. customThe obtained reaction mixture
  2. customwas purified by silica gel column chromatography

출처 및 근거

ORD 기록
ord-191b20a89f0f462bb79b6e61e3e18961
출처 데이터셋
uspto-grants-2015_08
특허 번호
US09115136B2

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