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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 460388Erstellt: 25. Oktober 2026

Methyl 3-hydroxy-4,5-dimethoxybenzoate → 1,4-Bis[5-(3-benzyloxy-4,5-dimethoxyphenyl)-2-pyridyl]hexahydro-1,4-diazepine

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Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktMethyl 3-hydroxy-4,5-dimethoxybenzoateHCID 2733956—
Edukt1,4-Bis(5-bromo-2-pyridyl)hexahydro-1,4-diazepineHCID 12991593—
Edukt(3-(Benzyloxy)-4,5-dimethoxyphenyl)boronic acidHCID 20634994—
Produkt1,4-Bis[5-(3-benzyloxy-4,5-dimethoxyphenyl)-2-pyridyl]hexahydro-1,4-diazepineHCID 20634961—

Reaktionsschritte

The procedure described in Example 31 was employed. From 1,4-bis(5-bromo-2-pyridyl)hexahydro-1,4-diazepine (115.0 mg, 0.280 mmol) synthesized in Reference Example 1 and 3-benzyloxy-4,5-dimethoxyphenylboronic acid (170.0 mg, 0.590 mmol) synthesized from methyl 3-hydroxy-4,5-dimethoxybenzoate (Indian J. Chem., 21B, 27–29, (1982)) by a similar procedure to that described in Reference Example 8, 1,4-bis[5-(3-benzyloxy-4,5-dimethoxyphenyl)-2-pyridyl]hexahydro-1,4-diazepine was obtained as a colorless viscous oil (173.0 mg, yield: 84%). From 1,4-bis[5-(3-benzyloxy-4,5-dimethoxyphenyl)-2-pyridyl]hexahydro-1,4-diazepine (157.0 mg, 0.210 mmol), 1,4-bis[5-(3-hydroxy-4,5-dimethoxyphenyl)-2-pyridyl]-hexahydro-1,4-diazepine was obtained as a colorless oil (97.0 mg, yield: 84%).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07196101B2
Quelldatensatzuspto-grants-2007_03
ORD IDord-34eb7ea1269148b5a1c2f1dff683d731
Quellennotizuspto-grants-2007_03