Morpholinoamidine → HCID 178517897, Verbindung

HRID 1507511

Reaktionsgleichung

Reaktionsgleichung von HRID 1507511
[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[CH:10]([C:16]([O:18]CC)=O)[C:11]([O:13]CC)=O.[N:21]1([C:27](=[NH:29])[NH2:28])[CH2:26][CH2:25][O:24][CH2:23][CH2:22]1>C1(C)C=CC=CC=1>[S:1]1[C:5]2[CH:6]=[CH:7][CH:8]=[CH:9][C:4]=2[N:3]=[C:2]1[C:10]1[C:11]([OH:13])=[N:28][C:27]([N:21]2[CH2:26][CH2:25][O:24][CH2:23][CH2:22]2)=[N:29][C:16]=1[OH:18]

Komponenten

4

Versuchsvorschrift

A mixture 1,3-diethyl 2-(1,3-benzothiazol-2-yl)propanedioate (3.00 g, 10.23 mmol, 1.00 equiv), and morpholine-4-carboximidamide (1.33 g, 10.30 mmol, 1.00 equiv) in Toluene (30 mL) was heated for 20 h at 120° C. under an inert atmosphere of nitrogen. After cooling down, the white solid was collected by filtration, washed with a mixture solution of Dichloromethane/Methanol and dried in an IR oven to afford the title compound. as a white solid. MS m/z [M+H]+ (ESI): 331.

Aufarbeitung

  1. temperatureAfter cooling down
  2. filtrationthe white solid was collected by filtration
  3. washwashed with a mixture solution of Dichloromethane/Methanol
  4. customdried in an IR oven

Quellen und Nachweise

ORD-Eintrag
ord-fc039b7d9efd457287a7034d818c6d6a
Quelldatensatz
uspto-grants-2015_12
Patentnummer
US09221809B2

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