Triethylamine → 3-Amino-2-oxo-1-phenylpyrrolidine-3-carboxylic acid (3-chloro-5-fluorobenzyl)amide

HRID 339605

Reaktionsgleichung

Reaktionsgleichung von HRID 339605
CCN(CC)CC.C(S)(S)CC.[Cl:13][C:14]1[CH:15]=[C:16]([CH:36]=[C:37]([F:39])[CH:38]=1)[CH2:17][NH:18][C:19]([C:21]1([N:33]=[N+]=[N-])[CH2:25][CH2:24][N:23]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:22]1=[O:32])=[O:20]>CO>[Cl:13][C:14]1[CH:15]=[C:16]([CH:36]=[C:37]([F:39])[CH:38]=1)[CH2:17][NH:18][C:19]([C:21]1([NH2:33])[CH2:25][CH2:24][N:23]([C:26]2[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=2)[C:22]1=[O:32])=[O:20]

Komponenten

5

Versuchsvorschrift

Et3N (0.1 ml, 0.75 mmol) followed by propanedithiol (0.08 ml, 0.75 mmol) are added to a solution of 3-azido-2-oxo-1-phenylpyrrolidine-3-carboxylic acid (3-chloro-5-fluorobenzyl)amide (100 mg, 0.25 mmol) in 2 ml of methanol. The batch is stirred at RT for 12 hours. When the reaction is complete, all volatile constituents are removed in vacuo, and the residue is purified on silica gel.

Aufarbeitung

  1. customall volatile constituents are removed in vacuo
  2. customthe residue is purified on silica gel

Quellen und Nachweise

ORD-Eintrag
ord-6d31dbd699b44efcac635c3acb941423
Quelldatensatz
uspto-grants-2014_11
Patentnummer
US08895535B2

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