Dimethylformamide → HCID 10602177, Verbindung

HRID 1653683

Reaktionsgleichung

Reaktionsgleichung von HRID 1653683
[CH3:1]N(C=O)C.[NH2:6][C:7]1[N:8]=[C:9]([NH2:27])[C:10]2[C:15]([CH2:16][CH2:17][C:18]3[CH:26]=[CH:25][C:21]([C:22](O)=[O:23])=[CH:20][CH:19]=3)=[CH:14][NH:13][C:11]=2[N:12]=1.[C:28]([O:32][C:33]([NH:35][CH2:36][CH2:37][CH2:38][C@@H:39]([C:41]([OH:43])=[O:42])[NH2:40])=[O:34])([CH3:31])([CH3:30])[CH3:29].P(C#N)(OCC)(OCC)=O>C(N(CC)CC)C>[NH2:6][C:7]1[N:8]=[C:9]([NH2:27])[C:10]2[C:15]([CH2:16][CH2:17][C:18]3[CH:26]=[CH:25][C:21]([C:22]([NH:40][C@H:39]([C:41]([O:43][CH3:1])=[O:42])[CH2:38][CH2:37][CH2:36][NH:35][C:33]([O:32][C:28]([CH3:31])([CH3:29])[CH3:30])=[O:34])=[O:23])=[CH:20][CH:19]=3)=[CH:14][NH:13][C:11]=2[N:12]=1

Komponenten

6

Versuchsvorschrift

To a DMF solution of 4-[2-(2,4-diamino-7H-pyrrolo [2,3-d]pyrimidin-5-yl)ethyl]benzoic acid (1.52 g) and methyl ester of N(δ)-t-butyloxycarbonyl-L-ornithine (1.3 g) was added diethyl cyanophosphate (1.4 g). The mixture was stirred for one hour at room temperature in the presence of triethylamine (3.0 g). The reaction mixture was concentrated under reduced pressure. The concentrate was purified by column chromatography on silica gel (carrier: 30 g; chloroform:ethanol containing 1% ammonium=20:1-15:1) to afford methyl N(α)-[4-[2-(2,4-diamino-7H-pyrrolo[2,3-d]pyrimidin-5-yl)ethyl]benzoyl]-N-(δ)-(t-butyloxycarbonyl)-L-ornithinate (2.30 g; yield 85%).

Aufarbeitung

  1. concentrationThe reaction mixture was concentrated under reduced pressure
  2. customThe concentrate was purified by column chromatography on silica gel (carrier: 30 g; chloroform:ethanol containing 1% ammonium=20:1-15:1)

Quellen und Nachweise

ORD-Eintrag
ord-6c87443a3ce54b5fa4461fbfe227b526
Quelldatensatz
uspto-grants-1995_04
Patentnummer
US05403843

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