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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900136Generated: October 29, 2026

m-Hydroxybenzohydrazide → HCID 58957933, compound

https://huagongshe.com/reaction/900136

Reaction equation

Participants

RoleNameHCIDCharge
Reactantm-HydroxybenzohydrazideHCID 79889—
Reactant2-(4-ethoxy-2-oxo-2,3-dihydro-benzo[b][1,4]diazepin-1-yl)-N-isopropyl-N-phenyl-acetamideHCID 58957936—
SolventAcetic AcidHCID 176—
ProductHCID 58957933HCID 58957933—

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 2-(4-ethoxy-2-oxo-2,3-dihydro-benzo[b][1,4]diazepin-1-yl)-N-isopropyl-N-phenyl-acetamide (Preparation 5(B) (177 mg, 0.466 mmol) in glacial acetic acid (4 mL) was added 3-hydroxy benzohydrazide (90 mg, 0.591 mmol). The reaction was heated to 120° C. for 3 hours, was cooled to room temperature, and was concentrated in vacuo. The residue was triturated with 50% Et2O in hexanes and the solids were filtered. The solids were dissolved in CH2Cl2 and the organic solution was washed with aqueous NaHCO3, dried (MgSO4) and concentrated to provide 244 mg of 2-[1-(3-hydroxy-phenyl)-5-oxo-4,5-dihydro-2,3,6,10b-tetraaza-benzo[e]azulen-6-yl]-N-isopropyl-N-phenyl-acetamide. 1H NMR (CD3OD) δ 7.74 (s, 2H), 7.56-7.18 (m, 10H), 6.91 (m, 1H), 4.86 (m, 1H), 4.30-4.10 (m, 2H), 3.98 (d, 1H), 3.71 (d, 1H), 1.06 (m, 6H).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07358242B2
Source datasetuspto-grants-2008_04
ORD IDord-f18ada96ac064f08a092f0545de8aa1e
Source noteuspto-grants-2008_04