Acetic Acid → 3-Methoxy-4-[2-(5-methyl-1,3,4-thiadiazol-2-yl)-3-oxobut-1-en-1-yl]benzonitrile

HRID 1951543ノート

反応式

HRID 1951543 の反応式
[CH3:1][C:2]1[S:6][C:5]([CH2:7][C:8]([CH3:10])=[O:9])=[N:4][N:3]=1.[CH:11]([C:13]1[CH:20]=[CH:19][C:16]([C:17]#[N:18])=[CH:15][C:14]=1[O:21][CH3:22])=O.N1CCCCC1.C(O)(=O)C>ClCCl>[CH3:22][O:21][C:14]1[CH:15]=[C:16]([CH:19]=[CH:20][C:13]=1[CH:11]=[C:7]([C:5]1[S:6][C:2]([CH3:1])=[N:3][N:4]=1)[C:8](=[O:9])[CH3:10])[C:17]#[N:18]

参加物

6

反応物 4

HCID 176Acetic AcidHCID 8082PiperidineHCID 131041141-(5-Methyl-1,3,4-thiadiazol-2-yl)propan-2-oneHCID 166592514-Formyl-3-methoxybenzonitrile

生成物 1

HCID 670179873-Methoxy-4-[2-(5-methyl-1,3,4-thiadiazol-2-yl)-3-oxobut-1-en-1-yl]benzonitrile

試薬・触媒・溶媒 1

HCID 6344Dichloromethane溶媒

実験手順

1.34 g (8.32 mmol) of 1-(5-methyl-1,3,4-thiadiazol-2-yl)acetone [T. Saito et al., J. Heterocycl. Chem. 20, 73-75 (1983)] and 1.30 g (8.32 mmol) of the compound from example 3A are dissolved in 20 ml of dichloromethane, and 0.165 ml (1.66 mmol) of piperidine and 0.100 ml (1.66 mmol) of acetic acid are added. The reaction mixture is heated under reflux with an inverse water trap overnight. The volatile components are removed in a rotary evaporator, and the crude product is purified by column chromatography (silica gel; eluent: initially dichloromethane, then cyclohexane/ethyl acetate 4:1→1:1). 1.17 g (47% of theory) of the title compound are obtained as a mixture of the E/Z isomers which can be crystallized from ethyl acetate/n-pentane. 530 mg of the title compound are obtained as a crystalline solid in this way.

後処理

  1. temperatureThe reaction mixture is heated
  2. temperatureunder reflux with an inverse water trap overnight
  3. customThe volatile components are removed in a rotary evaporator
  4. customthe crude product is purified by column chromatography (silica gel

出典と根拠

ORDレコード
ord-67c269a490874675afa8e8a1c726ad43
出典データセット
uspto-grants-2013_03
特許番号
US08404723B2

反応ノート

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