Hydrochloric Acid → 4-[4-(1,2-Benzisothiazol-3-yl)-1-piperazinyl]-1-(4-fluorophenyl)-1-butanone hydrochloride

HRID 648200ノート

反応式

HRID 648200 の反応式
[Cl:1][CH2:2][CH2:3][CH2:4][C:5]1([C:11]2[CH:16]=[CH:15][C:14]([F:17])=[CH:13][CH:12]=2)[O:10]CCCO1.[N:18]1([C:24]2[C:28]3[CH:29]=[CH:30][CH:31]=[CH:32][C:27]=3[S:26][N:25]=2)[CH2:23][CH2:22][NH:21][CH2:20][CH2:19]1.C(=O)([O-])[O-].[K+].[K+].[I-].[K+].Cl>C(#N)C.C(O)C>[ClH:1].[S:26]1[C:27]2[CH:32]=[CH:31][CH:30]=[CH:29][C:28]=2[C:24]([N:18]2[CH2:19][CH2:20][N:21]([CH2:2][CH2:3][CH2:4][C:5]([C:11]3[CH:12]=[CH:13][C:14]([F:17])=[CH:15][CH:16]=3)=[O:10])[CH2:22][CH2:23]2)=[N:25]1

参加物

8

実験手順

Title product hydrochloride. A mixture of 2-(3-chloropropyl)-2-(4-fluorophenyl)-1,3-dioxane (4.31 g., 0.0176 mole), 3-(1-piperazinyl)-1,2-benzisothiazole (3.86 g., 0.0176 mole), powdered potassium carbonate (2.43 g., 0.0176 mole) and potassium iodide (0.88 g., 0.0053 mole) in 180 ml. of dry acetonitrile is refluxed for a 20 hr. period. The reaction mixture is filtered, concentrated in vacuo and residual oil dissolved in chloroform and filtered. Concentration of the filtrate affords an oily residue which is taken up in 100 ml. of ethanol containing 10 ml. of 3 N hydrochloric acid and refluxed for 15 min. period. Acetonitrile is added to the cooled mixture and the solid obtained collected, 3.3 g. m.p. 248°-250° C. Crystallization of this material from ethanol affords analytically pure 4-[4-(1,2-benzisothiazol-3-yl)-1-piperazinyl]-1-(4-fluorophenyl)-1-butanone hydrochloride, m.p. 251°-254° C.

後処理

  1. filtrationThe reaction mixture is filtered
  2. concentrationconcentrated in vacuo and residual oil
  3. dissolutiondissolved in chloroform
  4. filtrationfiltered
  5. customConcentration of the filtrate affords an oily residue which
  6. customthe solid obtained
  7. customcollected
  8. customCrystallization of this material from ethanol

出典と根拠

ORDレコード
ord-c2e0f8871274434ba9e94083c1669b26
出典データセット
uspto-grants-1983_10
特許番号
US04411901

反応ノート

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