Hydrochloric Acid → 2,1,3-Benzothiadiazole, 4-(1-piperazinyl)-

HRID 1639274ノート

反応式

HRID 1639274 の反応式
[N:1]1[S:2][N:3]=[C:4]2[C:9]([N:10]3[CH2:15][CH2:14][N:13](C(OC=C)=O)[CH2:12][CH2:11]3)=[CH:8][CH:7]=[CH:6][C:5]=12.Cl>C(O)C>[N:1]1[S:2][N:3]=[C:4]2[C:9]([N:10]3[CH2:15][CH2:14][NH:13][CH2:12][CH2:11]3)=[CH:8][CH:7]=[CH:6][C:5]=12

参加物

4

反応物 2

HCID 313Hydrochloric AcidHCID 14581394HCID 14581394、化合物

生成物 1

HCID 114245542,1,3-Benzothiadiazole, 4-(1-piperazinyl)-

試薬・触媒・溶媒 1

HCID 702Ethanol溶媒

実験手順

To a 50 ml round-bottomed flask equipped with condenser and N2 inlet were added 530 mg (1.83 mmol) 4-(2,1,3-benzothiadiazolyl)-N-vinyloxycarbonylpiperazine and 25 ml ethanol, and the suspension saturated with HCl gas. The reaction was refluxed 2.75 hours, cooled, and evaporated. The residue was triturated with acetone to give a yellow solid N-(2,1,3-benzothiadiazolyl)-piperazine, m.p. 240°-244° C., 365 mg (62%).

後処理

  1. customTo a 50 ml round-bottomed flask equipped with condenser and N2 inlet
  2. temperatureThe reaction was refluxed 2.75 hours
  3. temperaturecooled
  4. customevaporated
  5. customThe residue was triturated with acetone

出典と根拠

ORDレコード
ord-b55dcee954374a5c8a16289375858681
出典データセット
uspto-grants-1989_11
特許番号
US04883795

反応ノート

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