Triethylamine → 3-(4-Benzylpiperazin-1-yl)propanethiol dihydrochloride

HRID 2290847

Reaktionsgleichung

Reaktionsgleichung von HRID 2290847
NC(N)=[S:3].[ClH:5].Cl.[CH2:7]([N:14]1[CH2:19][CH2:18][N:17]([CH2:20][CH2:21][CH2:22][Cl:23])[CH2:16][CH2:15]1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1.C(N(CC)CC)C.[OH-].[Na+]>O.C(O)C>[ClH:23].[ClH:5].[CH2:7]([N:14]1[CH2:19][CH2:18][N:17]([CH2:20][CH2:21][CH2:22][SH:3])[CH2:16][CH2:15]1)[C:8]1[CH:13]=[CH:12][CH:11]=[CH:10][CH:9]=1

Komponenten

7

Versuchsvorschrift

15 g of thiourea were added to a solution of 35 g of 1-benzyl-4-(3-chloropropyl)piperazine dihydrochloride, 20 g of triethylamine and 250 ml of reagent ethanol, and the mixture was refluxed for 8 hours. After the addition of a solution of 10 g of sodium hydroxide in 50 ml of water, the resulting mixture was refluxed for 4 additional hours. The ethanol was removed in vacuo, and water added to the residue which was extracted with methylene chloride, dried (sodium sulfate), and the salt was precipitated with ethereal hydrochloric acid to give 25.1 g (78% of theory) of 3-(4-benzylpiperazin-1-yl)propanethiol dihydrochloride as a white crystalline solid, M.p. 270°-273° C. (dec.).

Aufarbeitung

  1. temperaturethe mixture was refluxed for 8 hours
  2. temperaturethe resulting mixture was refluxed for 4 additional hours
  3. customThe ethanol was removed in vacuo, and water
  4. additionadded to the residue which
  5. extractionwas extracted with methylene chloride
  6. dry with materialdried (sodium sulfate)
  7. customthe salt was precipitated with ethereal hydrochloric acid

Quellen und Nachweise

ORD-Eintrag
ord-bd16d46356f54e52ade0e7d429a9301d
Quelldatensatz
uspto-grants-1986_10
Patentnummer
US04618677

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