tert-Butyl isothiocyanate → N-(tert-butyl)-N'-[2-hydroxy-1-(4-methyl-piperazin-1-ylmethyl)ethyl]thiourea

HRID 966950

Reaktionsgleichung

Reaktionsgleichung von HRID 966950
Cl.[NH2:2][CH:3]([CH2:6][N:7]1[CH2:12][CH2:11][N:10]([CH3:13])[CH2:9][CH2:8]1)[CH2:4][OH:5].[C:14]([N:18]=[C:19]=[S:20])([CH3:17])([CH3:16])[CH3:15]>C(O)C.C(N(CC)CC)C.O.ClCCl>[C:14]([NH:18][C:19]([NH:2][CH:3]([CH2:6][N:7]1[CH2:8][CH2:9][N:10]([CH3:13])[CH2:11][CH2:12]1)[CH2:4][OH:5])=[S:20])([CH3:17])([CH3:16])[CH3:15]

Komponenten

7

Edukt 2

HCID 11544tert-Butyl isothiocyanateHCID 222939172-Amino-3-(4-methyl-piperazinyl)-1-propanol, hydrochloride

Produkt 1

HCID 9814494N-(tert-butyl)-N'-[2-hydroxy-1-(4-methyl-piperazin-1-ylmethyl)ethyl]thiourea

Reagenzien, Katalysatoren, Lösungsmittel 4

HCID 702EthanolLösungsmittelHCID 962WaterLösungsmittelHCID 6344DichloromethaneLösungsmittelHCID 8471TriethylamineLösungsmittel

Reaktionsbedingungen

Temperatur
20 °C

Versuchsvorschrift

To a solution of 1 g of 2-amino-3-(4-methyl-piperazin1-yl)-1-propanol hydrochloride in 20 mL of absolute ethanol and 1.43 mL of triethylamine, about 0.78 mL of tert-butylisothiocyanate are added. The reaction mixture is stirred under inert atmosphere at a temperature of about 20° C. for 42 hours then is heated at a temperature of about 50° C. for 1 hour 30 min. After cooling at a temperature of about 20° C., the reaction medium is evaporated under reduced pressure (2 kPa) at a temperature of about 30° C. The residue thus obtained is taken up in 10 mL of water and 40 mL of dichloromethane. The aqueous phase is extracted with 2 times 30 mL of dichloromethane. The organic phases are collected, washed with 15 mL of water, dried over magnesium sulfate, filtered, then concentrated under reduced pressure (2 kPa) at a temperature of about 20° C. About 0.42 g of N-(tert-butyl)-N′-[2-hydroxy-1-(4-methyl-piperazin-1-ylmethyl)ethyl]thiourea are obtained in the form of a white paste. [Infrared spectrum between lamella of KBr 3279; 3075; 2939; 2806; 1533; 1459; 1359; 1295; 1204; 1010 and 821 cm−1].

Aufarbeitung

  1. temperaturethen is heated at a temperature of about 50° C. for 1 hour 30 min
  2. temperatureAfter cooling at a temperature of about 20° C.
  3. customthe reaction medium is evaporated under reduced pressure (2 kPa) at a temperature of about 30° C
  4. customThe residue thus obtained
  5. extractionThe aqueous phase is extracted with 2 times 30 mL of dichloromethane
  6. customThe organic phases are collected
  7. washwashed with 15 mL of water
  8. dry with materialdried over magnesium sulfate
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure (2 kPa) at a temperature of about 20° C

Quellen und Nachweise

ORD-Eintrag
ord-0b5eb9b5cfab41fabecfaafda32e1dea
Quelldatensatz
uspto-grants-2005_10
Patentnummer
US06953796B2

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