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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 900126Erstellt: 25. Oktober 2026

Ethyl Acetate → 1-cyclohexyl-4H,6H-2,3,6,10b-tetraaza-benzo[e]azulen-5-one

https://huagongshe.com/reaction/900126

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktEthyl AcetateHCID 8857—
EduktCyclohexanecarbohydrazideHCID 240039—
EduktSodium BicarbonateHCID 516892—
Edukt2H-1,5-Benzodiazepin-2-one, 4-ethoxy-1,3-dihydro-HCID 58957915—
LösungsmittelAcetic AcidHCID 176—
LösungsmittelWaterHCID 962—
LösungsmittelDiethyl EtherHCID 3283—
Produkt1-cyclohexyl-4H,6H-2,3,6,10b-tetraaza-benzo[e]azulen-5-oneHCID 58957932—

Reaktionsbedingungen

Temperatur120 °C

Reaktionsschritte

To a solution of 4-ethoxy-1,3-dihydro-benzo[b][1,4]diazepin-2-one (Preparation 3(A) (5 g, 24.5 mmol) in glacial acetic acid (75 mL) was added cyclohexanecarboxylic acid hydrazide (Preparation 14) (3.5 g, 24.5 mmol). The reaction was heated at 120° C. for 2.5 hours, was cooled to room temperature, and EtOAc (50 mL), water (50 mL) and aqueous NaHCO3 (50 mL) were added. The mixture was stirred for 5 minutes and Et2O was added (125 mL). The suspension was stirred for 15 minutes and the solids were removed by filtration with the aid of Et2O to provide 5.92 g of 1-cyclohexyl-4H,6H-2,3,6,10b-tetraaza-benzo[e]azulen-5-one. 1H NMR (CDCl3) δ 8.36 (s, NH), 7.50 (m, 1H), 7.41 (m, 2H), 7.30 (d, 1H), 4.13 (d, 1H), 3.47 (d, 1H), 2.87 (m, 1H), 2.24 (d, 1H), 2.00 (m, 2H), 1.72-1.51 (m, 4H), 1.33 (m, 2H), 1.16 (m, 1H); MS 283.4 (M+1), 281.3 (M−1).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS07358242B2
Quelldatensatzuspto-grants-2008_04
ORD IDord-681642658a624ab3927ac4f4c3b58618
Quellennotizuspto-grants-2008_04