HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 900136Generated: October 29, 2026
m-Hydroxybenzohydrazide → HCID 58957933, compound
https://huagongshe.com/reaction/900136
Participants
| Role | Name | HCID | Charge |
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| Reactant | m-Hydroxybenzohydrazide | HCID 79889 | — |
| Reactant | 2-(4-ethoxy-2-oxo-2,3-dihydro-benzo[b][1,4]diazepin-1-yl)-N-isopropyl-N-phenyl-acetamide | HCID 58957936 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Product | HCID 58957933 | HCID 58957933 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07358242B2 |
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| Source dataset | uspto-grants-2008_04 |
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| ORD ID | ord-f18ada96ac064f08a092f0545de8aa1e |
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| Source note | uspto-grants-2008_04 |
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