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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2214535Erstellt: 24. Oktober 2026

Formaldehyde → N-[(3,4-dichlorophenyl)methyl]-4-hydroxy-N-methyl-1-[2-(3-morpholinopropanoylamino)ethyl]-5-oxo-2H-pyrrole-3-carboxamide

https://huagongshe.com/de/reaction/2214535

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktFormaldehydeHCID 712—
EduktN-(2-amino-ethyl)-3-morpholin-4-yl-propionamideHCID 21947517—
Edukt3-[3-[3-[(3,4-dichlorophenyl)methyl-methyl-carbamoyl]-4-hydroxy-5-oxo-2H-pyrrol-1-yl]propanoylamino]propanoic acidHCID 54691726—
EduktN-(3,4-Dichloro-benzyl)-2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-N-methyl-acetamideHCID 69655735—
ProduktN-[(3,4-dichlorophenyl)methyl]-4-hydroxy-N-methyl-1-[2-(3-morpholinopropanoylamino)ethyl]-5-oxo-2H-pyrrole-3-carboxamideHCID 54698208—

Reaktionsschritte

N-(3,4-Dichloro-benzyl)-2-(2,2-dimethyl-5-oxo-[1,3]dioxolan-4-ylidene)-N-methyl-acetamide (Compound 37-A) was treated with paraformaldehyde and N-(2-amino-ethyl)-3-morpholin-4-yl-propionamide as described in the preparation of Compound 37. The desired product was isolated as a white solid (0.0134 g, 5% yield). 1H NMR (300 MHz, CDCl3) δ: 2.41 (m, 2H), 2.64 (bs, 2H), 2.72 (bs, 2H), 2.98 (m, 2H), 3.03 (s, 3H), 3.51 (t, J=5.6 Hz, 2H), 3.63 (t, J=5.2 Hz, 2H), 3.78 (m, 4H), 4.35 (s, 2H), 4.59 (s, 2H), 7.11 (d, J=8.1 Hz, 1H), 7.35–7.44 (m, 3H), 8.27 (t, 1H). HRMS (M+H) calcd for C22H28N4Cl2O5: 497.13585. found: 497.1377.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07109186B2
Quelldatensatzuspto-grants-2006_09
ORD IDord-b4c4d6cde14149838ceb9363e1ac4cef
Quellennotizuspto-grants-2006_09