1-Phenethylamine, (-)- → HCID 178462014, Verbindung

HRID 539611Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 539611
FC1C=CC=C(F)C=1O[C:5]1[O:6][C:7]([CH3:16])([CH3:15])[C:8]([CH3:14])([CH3:13])[S:9](=[O:12])(=[O:11])[N:10]=1.[C:22]1([C@@H:28]([NH2:30])[CH3:29])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1>>[C:22]1([C@@H:28]([NH:30][C:5]2[O:6][C:7]([CH3:15])([CH3:16])[C:8]([CH3:13])([CH3:14])[S:9](=[O:11])(=[O:12])[N:10]=2)[CH3:29])[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1

Komponenten

3

Edukt 2

HCID 758181-Phenethylamine, (-)-HCID 867054542-(2,6-Difluorophenoxy)-5,5,6,6-tetramethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide

Produkt 1

HCID 178462014HCID 178462014, VerbindungAusbeute 50,9 %

Versuchsvorschrift

A mixture of 194 mg of 2-(2,6-difluorophenoxy)-5,5,6,6-tetramethyl-5,6-dihydro-1,4,3-oxathiazine 4,4-dioxide and 737 mg of (S)-1-phenylethylamine was stirred at room temperature for 16 hours and then purified in a purification laboratory by means of preparative HPLC. The combined product-containing fractions were alkalized with 25% aqueous ammonia solution and extracted three times with 30 ml of ethyl acetate, and the combined organic phases were dried over MgSO4 and concentrated by rotary evaporation. This gave the product (96 mg) with a molecular weight of 310.4 g/mol (C15H22N2O3S); MS (ESI): m/e=311 (M+H+).

Aufarbeitung

  1. custompurified in a purification laboratory by means of preparative HPLC
  2. additionThe combined product-containing fractions
  3. extractionextracted three times with 30 ml of ethyl acetate
  4. dry with materialthe combined organic phases were dried over MgSO4
  5. concentrationconcentrated by rotary evaporation

Quellen und Nachweise

ORD-Eintrag
ord-da46496f2c4848c3b900356353f84c50
Quelldatensatz
uspto-grants-2014_10
Patentnummer
US08871758B2

Notizen zur Reaktion

Wird geladen…