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Diphenyl Ether → 4-Oxo-4,5-dihydrothieno[3,2-c]pyridine-7-carbonitrile

HRID 1868292
ノート
印刷プレビュー

反応式

HRID 1868292 の反応式
C1([O:7][C:8]2C=CC=CC=2)C=CC=CC=1.C([N:18](CCCC)CCCC)CCC.[C:27]([C:29]([C:36]1[S:37][CH:38]=[CH:39][CH:40]=1)=[CH:30]C(N=[N+]=[N-])=O)#[N:28]>C(Cl)Cl>[O:7]=[C:8]1[C:40]2[CH:39]=[CH:38][S:37][C:36]=2[C:29]([C:27]#[N:28])=[CH:30][NH:18]1
参加物反応条件実験手順後処理出典と根拠反応ノート

参加物

5

反応物 3

HCID 7583Diphenyl EtherHCID 7622TributylamineHCID 73446014HCID 73446014、化合物

生成物 1

HCID 184465784-Oxo-4,5-dihydrothieno[3,2-c]pyridine-7-carbonitrile

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

反応条件

温度
212.5 °C

実験手順

To a stirring solution of diphenyl ether (1.5 L) and trin-butylamine (0.3 L) heated to an equilibrated temperature of 215° C. was dropwise added a solution of 3-cyano-3-thiophen-2-yl-acryloyl azide 23 (85 g, 0.416 mol) in CH2Cl2 (340 mL). The temperature was maintained between 210-215° C. during this time. Following addition, the reaction was stirred a further 30 min, then allowed to cool to room temperature, during which the pure product precipitated from solution. The product was filtered and washed with copious hexane. Drying the precipitate under vacuum provided 58.4 g of 24. 1H NMR (400 MHz, d6-DMSO) δ 12.36 (s, 1H), 8.27 (s, 1H), 7.81 (d, J=5 Hz, 1H), 7.57 (d, J=5 Hz 1H).

後処理

  1. additionaddition
  2. temperatureto cool to room temperature, during which the pure product
  3. customprecipitated from solution
  4. filtrationThe product was filtered
  5. washwashed with copious hexane
  6. customDrying the precipitate under vacuum

出典と根拠

ORDレコード
ord-d93e2f0a35c34fbaa2eed59495218158
出典データセット
uspto-grants-2009_12
DOI
10.6084/m9.figshare.5104873.v1
特許番号
US07635695B2

反応ノート

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