Isopropylamine → HCID 86661277, Verbindung

HRID 1685008Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1685008
[Cl:1][C:2]1[CH:3]=[C:4]([CH:17]=[CH:18][C:19]=1[Cl:20])[CH2:5][NH:6][C:7]([NH:9][C:10]1[S:11][CH:12]=[C:13]([CH2:15]I)[N:14]=1)=[O:8].[CH:21]([NH2:24])([CH3:23])[CH3:22]>O1CCCC1>[Cl:1][C:2]1[CH:3]=[C:4]([CH:17]=[CH:18][C:19]=1[Cl:20])[CH2:5][NH:6][C:7]([NH:9][C:10]1[S:11][CH:12]=[C:13]([CH2:15][NH:24][CH:21]([CH3:23])[CH3:22])[N:14]=1)=[O:8]

Komponenten

4

Edukt 2

HCID 6363IsopropylamineHCID 58055059HCID 58055059, Verbindung

Produkt 1

HCID 86661277HCID 86661277, Verbindung

Reagenzien, Katalysatoren, Lösungsmittel 1

HCID 8028TetrahydrofuranLösungsmittel

Versuchsvorschrift

The 1-(3,4-Dichloro-benzyl)-3-(4-iodomethyl-thiazol-2-yl)-urea intermediate (0.3 mmol) was taken up in tetrahydrofuran (5 ml) and isopropyl amine (20 eq.) was added. The reaction was stirred overnight at room temperature. Added a saturated solution of NaSO3 (40 ml). Extracted this with EtOAc twice. The combined organic extracts were dried over Na2SO4, filtered and solvent removed in vacuo. The crude 1-(3,4-dichlorobenzyl)-3-(4-((isopropylamino)methyl)thiazol-2-yl)urea was used as is.

Aufarbeitung

  1. extractionExtracted this with EtOAc twice
  2. dry with materialThe combined organic extracts were dried over Na2SO4
  3. filtrationfiltered
  4. customsolvent removed in vacuo

Quellen und Nachweise

ORD-Eintrag
ord-bec7f25a0b004b0f8d13a8dbeceae07b
Quelldatensatz
uspto-grants-2012_04
Patentnummer
US08148380B2

Notizen zur Reaktion

Wird geladen…