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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 14693Erstellt: 24. Oktober 2026

O-Phenylenediamine → (1-Aminomethyl-6,8-dimethoxy-isoquinolin-4-yl)-(1h-benzoimidazol-2-yl)-amine

https://huagongshe.com/de/reaction/14693

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktO-PhenylenediamineHCID 7243—
EduktTriethylamineHCID 8471—
EduktThiophosgeneHCID 10040—
Edukt2-(4-Amino-6,8-dimethoxy-isoquinolin-1-ylmethyl)-isoindole-1,3-dioneHCID 59341090—
KatalysatorMercuric oxideHCID 30856—
LösungsmittelDichloromethaneHCID 6344—
Produkt(1-Aminomethyl-6,8-dimethoxy-isoquinolin-4-yl)-(1h-benzoimidazol-2-yl)-amineHCID 4684753950,6%

Reaktionsschritte

Triethylamine (210 μL, 1.52 mmol) and then thiophosgene (55 μL, 0.72 mmol) were added to a solution of Example 45C (200 mg, 0.55 mol) in dichloromethane (5 mL), and the reaction stirred 1 h at r.t. Organics were washed with 0.5 N HCl and brine, dried (MgSO4), and concentrated. The residue was dissolved in DMF (5 mL). Phenylenediamine (89 mg, 0.82 mmol) was added, and the reaction stirred at 90° C. for 2 h. Mercury(II) oxide was added, and the reaction stirred for 3 h longer before it was concentrated in vacuo. Deprotection was carried out in ethanol (5 mL) with hydrazine (0.2 mL) at r.t. for 1 h. Purification by Prep-HPLC gave 145 mg (46%) of the title compound (TFA salt) as a yellow solid. H1-NMR (MeOD-d4): δ 8.61 (s, 1H), 7.38-7.42 (m, 2H), 7.30-7.34 (m, 2H), 7.23 (s, 1H); 7.02 (d, 1H, J=2.0 Hz), 6.89 (d, 1H, J=2.0 Hz), 4.92 (s, 2H), 4.01 (s, 3H), 3.91 (s, 3H). MS (ES) (M+H) calc'd for C19H19N5O2, 350; found 350.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07732446B1
Quelldatensatzuspto-grants-2010_06
ORD IDord-ef59f10e08574a5fb9503363bad1cfd1
Quellennotizuspto-grants-2010_06