HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetic Acid → Acetamide, N-[10-(1,3-benzodioxol-5-yl)-7,9-dihydro-7,9-dioxo-8H-1,3-benzodioxolo[4,5-f]isoindol-8-yl]-
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Hydrazine hydrate (1:1) | HCID 24654 | — |
| Reactant | 10-Benzo[1,3]dioxol-5-yl-furo[3',4':6,7]naphtho[1,2-d][1,3]dioxole-7,9-dione | HCID 5273777 | — |
| Product | Acetamide, N-[10-(1,3-benzodioxol-5-yl)-7,9-dihydro-7,9-dioxo-8H-1,3-benzodioxolo[4,5-f]isoindol-8-yl]- | HCID 5273798 | 86% |
Reaction Steps
A solution of anhydride 1 (145 mg, 0.4 mmol) in glacial acetic acid (10 mL) was refluxed with hydrazine hydrate (0.023 mL, 0.48 mmol) for 24 h under nitrogen and then poured, after cooling, into ice water. The resulting precipitate was filtered and dried under reduced pressure. The residue was purified by column chromatography on silica gel using CH2Cl2/MeOH (30:1 to 20:1, v/v) to give 25 (143 mg, 86%) as a yellow solid. mp 281-283° C.; 1H NMR (CDCl3) δ 8.34 (s, 1H, H4), 7.69 (d, 1H, H5, J=8.7 Hz), 7.46 (s, 1H, NHAc), 7.38 (d, 1H, H6, J=8.7 Hz), 6.84-6.87 (m, 3H, H2′+H5′+H6′), 6.06 (AB, 2H, 3′,4′-OCH2O—, Δδ=16.5 Hz, J=1.5 Hz), 5.98 (AB, 2H, 7,8-OCH2O—, Δδ=5.4 Hz, J=1.2 Hz), 2.17 (s, 3H, NHCOCH3); MS (EI) m/z 418 [M]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07754718B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-9982b5b4fa1d45f6b2d0c2467f1f04fb |
| Source note | uspto-grants-2010_07 |