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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 55014Erstellt: 24. Oktober 2026

1-Bromomethyl-2,6-dichlorobenzene → 1-(2,6-Dichlorobenzyl)-3-[1-(6,7-dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxoquinazoline

https://huagongshe.com/de/reaction/55014

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt1-Bromomethyl-2,6-dichlorobenzeneHCID 30159—
Edukt3-[1-(6,7-Dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxoquinazolineHCID 22923399—
Produkt1-(2,6-Dichlorobenzyl)-3-[1-(6,7-dimethoxy-4-quinazolinyl)-4-piperidinyl]-1,2,3,4-tetrahydro-6-nitro-2,4-dioxoquinazolineHCID 2292355529%

Reaktionsschritte

The procedure similar to that described in Example 1 was repeated, except that 300 mg (0.63 mmol) of Compound 24 was used and 2,6-dichlorobenzyl bromide was used in place of methyl iodide. As a result, 117.1 mg (yield: 29%) of Compound 10 was obtained as pale yellow crystals.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05624926
Quelldatensatzuspto-grants-1997_04
ORD IDord-c9f7607c9cc145cbb5f7356aba12dec0
Quellennotizuspto-grants-1997_04