Dicyclohexylcarbodiimide → HCID 178512917, Verbindung

HRID 420431Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 420431
C1C=CC2N(O)N=NC=2C=1.C(N(C(C)C)CC)(C)C.Cl.[CH2:21]([O:28][C:29]([NH:31][C@H:32]([C:40]([OH:42])=[O:41])[CH2:33][CH2:34][CH2:35][NH:36][C:37](=[NH:39])[NH2:38])=[O:30])[C:22]1[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=1.C1(N=C=NC2CCCCC2)CCCCC1>CN(C=O)C>[NH:31]([C:29]([O:28][CH2:21][C:22]1[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=1)=[O:30])[C@H:32]([C:40]([OH:42])=[O:41])[CH2:33][CH2:34][CH2:35][NH:36][C:37](=[NH:38])[NH2:39]

Komponenten

6

Versuchsvorschrift

The amino-component (10 mmol) was dissolved in DMF (70 ml), and 4,59 g (30 mmol monohydrate) HOBT was added. To the solution was diisopropyletylamine (DIPEA) added dropwise, until the pH of the mixture, controlled with wet indicator paper reached 7-8. Next, the N-benzyloxycarbonyl-arginine hydrochloride (5.17 g, 15 mmol) was added and the solution was cooled on ice bath. N,N′-Dicyclohexylcarbodiimide (3.09 g, 15 mmol) was added in small portions during 1 h. and after additional 1 h of stirring, the reaction mixture was left in a cold room overnight (approximately 4° C.). The precipitated DCU was filtered off and washed with a small volume of DMF and the combined filtrates were evaporated under reduced pressure. From the resulting mixture A20 (or its analogues) was isolated using chromatography techniques.

Aufarbeitung

  1. additionadded dropwise, until the pH of the mixture
  2. temperaturethe solution was cooled on ice bath
  3. filtrationThe precipitated DCU was filtered off
  4. washwashed with a small volume of DMF
  5. customthe combined filtrates were evaporated under reduced pressure
  6. customFrom the resulting mixture A20 (or its analogues) was isolated

Quellen und Nachweise

ORD-Eintrag
ord-5b4f98f3cfaa4de09a479c949880c914
Quelldatensatz
uspto-grants-2012_01
Patentnummer
US08097582B2

Notizen zur Reaktion

Wird geladen…