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1-Hydroxybenzotriazole → HCID 178454187, Verbindung

HRID 555436
Notizen
Druckvorschau

Reaktionsgleichung

Reaktionsgleichung von HRID 555436
C1C2C(=CC=CC=2)C=C(C2C=CC(O)=CC=2)N=1.C1C=CC2N(O)N=NC=2C=1.[CH3:28][C:29]([O:32][C:33]([NH:35][C@H:36]([C:58]([OH:60])=[O:59])[CH2:37][CH2:38][CH2:39][N:40]=[C:41]([NH:50]C(OC(C)(C)C)=O)[NH:42]C(OC(C)(C)C)=O)=[O:34])([CH3:31])[CH3:30].CCN=C=NCCCN(C)C.Cl.C(N(CC)C(C)C)(C)C>CN(C=O)C.O>[C:33]([NH:35][C@H:36]([C:58]([OH:60])=[O:59])[CH2:37][CH2:38][CH2:39][NH:40][C:41](=[NH:42])[NH2:50])([O:32][C:29]([CH3:30])([CH3:28])[CH3:31])=[O:34]
KomponentenVersuchsvorschriftAufarbeitungQuellen und NachweiseNotizen zur Reaktion

Komponenten

8

Edukt 5

HCID 757711-HydroxybenzotriazoleHCID 81531DiisopropylethylamineHCID 27239391,3-Propanediamine, N'-(ethylcarbonimidoyl)-N,N-dimethyl-, monohydrochlorideHCID 11385959Boc-arg(boc)2-OHHCID 1354251244-(Isoquinolin-3-yl)phenol

Produkt 1

HCID 178454187
HCID 178454187, Verbindung
Ausbeute 182,3 %

Reagenzien, Katalysatoren, Lösungsmittel 2

HCID 962WaterLösungsmittelHCID 6228DimethylformamideLösungsmittel

Versuchsvorschrift

To a solution of 4-isoquinolin-3-yl-phenol (0.133 g, 0.6 mmol) in anhydrous DMF (5 mL) were added HOBt (0.081 g, 0.6 mmol), Boc-Arg-(Boc)2-OH (0.285 g, 0.6 mmol), and EDCl (0.115 g, 0.6 mmol). N,N-Diisopropyl ethyl amine (0.233 g, 1.8 mmol) was added and the mixture was stirred at room temperature for 24 h. Water (15 mL) was added and the white precipitate was filtered off, washed with water and dried under vacuum to give 0.3 g (74%) of the Boc-arginine derivative. The above compound (0.3 g) was dissolved in anhydrous dichloromethane (10 mL). HCl gas was bubbled into the solution at 0° C. for 4 h. A yellow precipitate was formed. The solvent was removed and the resulting solid was dried under vacuum. Triturating with ether gave 4-(isoquinolin-3-yl)phenyl 2-amino-5-guanidinopentanoate tetrahydrochloride (0.2 g, 86%). Selected data: MS (ES) m/z: 222.96 (M+1−Arg), 221.99 (M−Arg); MP 198-201° C.

Aufarbeitung

  1. filtrationthe white precipitate was filtered off
  2. washwashed with water
  3. customdried under vacuum

Quellen und Nachweise

ORD-Eintrag
ord-58b7be0452e2464394024125cb01af2f
Quelldatensatz
uspto-grants-2011_11
DOI
10.6084/m9.figshare.5104873.v1
Patentnummer
US08053440B2

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