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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 343191Erstellt: 25. Oktober 2026

Hydrochloric Acid → 2-(2,4-Dioxo-5-phenyl-3-methyl-3-phenylcarbamoylmethyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-N-isopropyl-N-phenyl acetamide

https://huagongshe.com/reaction/343191

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktHydrochloric AcidHCID 313—
EduktAnilineHCID 6115—
EduktDiisopropylethylamineHCID 81531—
EduktPyBroPHCID 2733179—
Edukt[1-(isopropyl-phenyl-carbamoylmethyl)-3-methyl-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl]acetic acidHCID 67696769—
Edukt{3-(Benzyloxycarbonyl-methyl)-1-[isopropyl-(4-methoxy-phenyl)-carbamoylmethyl]-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl}acetic acidHCID 86753587—
LösungsmittelDimethylformamideHCID 6228—
Produkt2-(2,4-Dioxo-5-phenyl-3-methyl-3-phenylcarbamoylmethyl-2,3,4,5-tetrahydro-benzo[b][1,4]diazepin-1-yl)-N-isopropyl-N-phenyl acetamideHCID 10031013—

Reaktionsschritte

A solution of 35 mg (0.07 mmol) of [1-(isopropyl-phenyl-carbamoylmethyl)-3-methyl-2,4-dioxo-5-phenyl-2,3,4,5-tetrahydro-1H-benzo[b][1,4]diazepin-3-yl]acetic acid, prepared as in Intermediate 7, 0.013 mL (0.14 mmol) of aniline, 66 mg (0.14 mmol) of PyBrOP and 0.05 mL (0.23 mmol) of N,N-diisopropyl-N-ethylamine in 2 mL of DMF is stirred at RT for 2 d. The reaction mixture is diluted with 30 mL of 1N HCl and extracted with EtOAc (×3). The organic extract is washed with 1N HCl, brine, sat. NaHCO3 and brine, dried over MgSO4 and concentrated in vacuo to a yellow oil. Purification by reverse phase C-18 MPLC (70% methanol/TFA-H2O) gave 16 mg of the title compound as a white powder; m.p. 228°-9° C.; 1H NMR (d6 -DMSO 300 MHz, mixture of conformations) δ9.73 (s, 1H), 7.6-7.2 (m, 16H), 7.05 (m, 2H), 6.65 (d, 1H, J=8), 4.85 (m, 1H), 4.22 (m, 2H), 2.33 (m, 2H), 1.20 (s, 3H), 1.00 (m, 6H); low resolution MS (FAB) m/e 575 (MH+).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05859007
Quelldatensatzuspto-grants-1999_01
ORD IDord-a71892a7589b4e19a57ae429ef76c23e
Quellennotizuspto-grants-1999_01