Piperazine → 6-Ethoxy-2-piperazin-1-yl-1,3-benzothiazole

HRID 1294780

Reaktionsgleichung

Reaktionsgleichung von HRID 1294780
Cl[C:2]1[S:3][C:4]2[CH:10]=[C:9]([O:11][CH2:12][CH3:13])[CH:8]=[CH:7][C:5]=2[N:6]=1.[NH:14]1[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]1.C(N(CC)CC)C>O1CCCC1>[CH2:12]([O:11][C:9]1[CH:8]=[CH:7][C:5]2[N:6]=[C:2]([N:14]3[CH2:19][CH2:18][NH:17][CH2:16][CH2:15]3)[S:3][C:4]=2[CH:10]=1)[CH3:13]

Komponenten

5

Edukt 3

HCID 4837PiperazineHCID 8471TriethylamineHCID 3500152-Chloro-6-ethoxybenzo[d]thiazole

Produkt 1

HCID 284708886-Ethoxy-2-piperazin-1-yl-1,3-benzothiazole

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Reaktionsbedingungen

Temperatur
160 °C

Versuchsvorschrift

A mixture of 1.36 mmol 2-chloro-6-ethoxy-benzothiazole (CA=[79071-17-3]), 3.00 mmol of piperazine and 3.00 mmol of triethylamine in 5 ml of tetrahydrofuran in a sealed tube was heated at 160° C. for 5 min under microwave irradiation. The reaction mixture was concentrated, and the residue was purified by chromatography (SiO2, methanol/dichloromethane) to yield the title compound as a white solid.

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated
  2. customthe residue was purified by chromatography (SiO2, methanol/dichloromethane)

Quellen und Nachweise

ORD-Eintrag
ord-ed6dfc162bde45228b20d9d792863b02
Quelldatensatz
uspto-grants-2007_07
Patentnummer
US07241761B2

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